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Recalls affecting Rhode Island

Data last updated: September 9, 2026 at 1:18 PM UTC

16,286 recalls found
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Just announced

Straight from FDA press releases — not yet formally classified or risk-graded
UnclassifiedUndeclaredAnnounced September 4, 2026

Business Pill, Branch Manager for Men — dietary supplements marketed for male sexual enhancement

Products contain undeclared yohimbine

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Dietary SupplementsFood & Beverages

Recalling firm: SUPPLX.com

Grant-Valkaria, Florida - SUPPLX.com is voluntarily recalling Business Pill and Branch Manager for Men, products marketed as dietary supplements for male sexual enhancement, because FDA laboratory analysis confirmed that both products contain yohimbine that is not declared on the product labels.

Company contact: (321) 341-9501 · SupplxRecall@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusSalmonellaAnnounced September 4, 2026

Foods Alive — Moringa Leaf Powder

Potential to be contaminated with Salmonella

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Food & BeveragesFoodborne Illness

Recalling firm: Foods Alive Inc.

Foods Alive Inc of Angola, IN, is recalling its 8-ounce packages of organic moringa leaf powder because they have the potential to be contaminated with Salmonella , an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

View FDA’s announcement (opens in a new tab)
UnclassifiedAnnounced September 3, 2026

B. Braun — 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container

Presence of particulate matter identified as iron oxide

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Drugs

Recalling firm: B. Braun Medical Inc.

“On September 3, 2026 firm updated their press release to include additional contaminants.” FOR IMMEDIATE RELEASE – September 3, 2026– Bethlehem, PA, B. Braun Medical Inc (B. Braun) is voluntarily recalling three (3) lots of 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container, to the hospital/healthcare facility/user level due to presence of particulate matter identified as iron…

Company contact: recalls@bbraunusa.com

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UnclassifiedBacteria/virusE. coliAnnounced September 3, 2026

Great Value — Organic Triple Berry Blend

Possible E. Coli Contamination

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Food & BeveragesFoodborne Illness

Recalling firm: Frutas y Hortalizas del Sur S.A.

September 02, 2026. Frutas y Hortalizas del Sur S.A., San Carlos, Chile expands its July 3, 2026, recall of frozen organic IQF blueberries to include one lot of Great Value frozen Organic Triple Berry Blend 10 OZ because of potential contamination with Escherichia coli O145:H28 (E. coli O145) .

Company contact: Info.foodsafety@comfrut.com

View FDA’s announcement (opens in a new tab)
UnclassifiedAnnounced September 3, 2026

American Regent, Inc. — Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vial

Presence of particulate matter and lack of sterility assurance

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Food & Beverages

Recalling firm: American Regent, Inc.

FOR IMMEDIATE RELEASE – September 3, 2026 – New Albany, OH, American Regent, Inc. is conducting a nationwide voluntary recall of three lots of Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vials to the consumer level. Customer complaints were received for leaking and cracked vials, resulting in lack of assurance of sterility.

View FDA’s announcement (opens in a new tab)
UnclassifiedAllergenMilkUndeclaredAnnounced August 31, 2026

Little Temptations — Chocolatey Eyeballs, 7 oz., 10 oz., 10.5 oz., 11 oz., and 16 oz.

Undeclared milk

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Food & BeveragesAllergens

Recalling firm: Crystal Temptations

Crystal Temptations of North Arlington, NJ is recalling Halloween Chocolatey Eyeballs because they contain undeclared MILK allergens. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume these products.

View FDA’s announcement (opens in a new tab)
UnclassifiedUndeclaredAnnounced August 31, 2026

Lipofit — Lipofit Extreme 2.0 Fat Burner Dietary Supplement

Undeclared Fluoxetine and 2,4-Dinitrophenol (DNP)

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Dietary SupplementsDrugs

Recalling firm: Ana Salazar Modela Tu Cuerpo Inc.

FOR IMMEDIATE RELEASE - August 27, 2026 - Davie, Florida – Ana Salazar Modela Tu Cuerpo Inc. is recalling Lipofit Extreme Fat Burner 2.0, Lot 25M12F, expiration date 09/2027, to the consumer level.

Company contact: (954) 305-1004 · yandrydy@gmail.com

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UnclassifiedAnnounced August 31, 2026

Kofinas — Garlic Mediterranean Infused Extra Virgin Olive Oil 500 ml, 250 ml, and 100 ml

Contains garlic essential oil not approved for culinary use

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Food & BeveragesIngredients

Recalling firm: LMSI LLC

Cincinnati, OH (Aug. 29, 2026) - LMSI LLC/ Kofinas Olive Oil is issuing a voluntary recall of its Garlic Mediterranean infused extra virgin olive oil for using a garlic essential oil not approved for culinary use. The flavored oil was bottled in glass bottles in 500 ml, 250 ml, and 100 ml sizes.

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusSalmonellaE. coliAnnounced August 29, 2026

Everything Sprouts — Robust Radish Mix, 5oz Cups

Potential to be contaminated with Shiga toxin-producing Escherichia coli (STEC) or Salmonella.

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Food & BeveragesFoodborne Illness

Recalling firm: Everything Sprouts, LLC

Everything Sprouts, LLC, based in Minneapolis, MN is expanding its voluntary recall of sprouts to include certain lots of Robust Radish Sprout Mix because it has the potential to be contaminated with Shiga toxin producing Escherichia coli (STEC) or Salmonella bacteria.

Company contact: everythingsproutsmn@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusSalmonellaAnnounced August 29, 2026

Martina — Mangoes

Potential contamination with Salmonella

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Food & BeveragesFoodborne Illness

Recalling firm: Panorama Produce

MAMARONECK, NY, AUG. 28, 2026 - Panorama Produce is recalling 302 boxes of size 9 (nine) mangoes because they may be contaminated with Salmonella , an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

Company contact: information@panoramaproduce.com

View FDA’s announcement (opens in a new tab)
Wording
UnclassifiedRisk not yet known
Medical deviceRecalled February 3, 2021

Implantable cardioverter defibrillators (ICD) with cardiac resynchronization therapy (CRT-D): 1) Viva family: Viva XT CRT-D, Viva XT Quad CRT-D, Viva S CRT-D, Viva Quad S CRT-D and Viva Quad C CRT-D models; 2) Claria family: Claria MRI CRT-D and Claria MRI Quad CRT-D models; 3) Amplia family: Amplia MRI CRT-D and Amplia MRI Quad CRT-D models; 4) Compia family: Compia MRI CRT-D model; 5) Brava family: Brava CRT-D and Brava Quad CRT-D models (OUS only); Implantable Cardioverter Defibrillators (ICDs) are implantable medical devices that automatically detect and treat episodes of ventricular fibrillation, ventricular tachycardia, fast ventricular tachycardia, and bradyarrhythmia. Some devices can also provide cardiac resynchronization therapy, including sequential biventricular pacing (CRT-D devices).

A small percentage of implanted cardiac devices, from a well-defined subset, may experience a shortened Recommended Replacement Time (RRT) to End of Service (EOS) interval following an earlier-than-expected RRT observation

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
87261
Lot/product code:
1) Viva family: MODEL NUMBER / NAME / GTIN: SERIAL NUMBERS BLF244376H, BLF243732H, BLF244567H, BLF243795H, BLF244186H, BLF244478H, BLF243894H, BLF243453H, BLF244610H, BLF244627H, BLF243514H, BLF242936H, BLF244189H, BLF243735H, BLF243429H, BLF244637H, BLF235234H, BLF242865H, BLF243129H, BLF243389H, BLF242685H, BLF243087H, BLF243671H, BLF243888H, BLF243897H, BLF244660H, BLF242664H, BLF242935H, BLF243975H, BLF243028H, BLF243445H, BLF243396H, BLF243947H, BLF243377H, BLF242659H, BLF244047H, BLF243393H, BLF243714H, BLF242861H, BLF243366H, BLF243378H, BLF242874H, BLF243382H, BLF243750H, BLF242082H, BLF242682H, BLF243363H, BLF243386H, BLF243413H, BLF243450H, BLF243452H, BLF243752H, BLF243513H, BLF243181H, BLF242551H, BLF243371H, BLF243772H, BLF241960H, BLF243455H, BLF243258H, BLF243391H, BLF243398H, BLF243401H, BLF243408H, BLF243055H, BLF244654H, BLF241810H, BLF242439H, BLF244207H, BLF243460H, BLF244390H, BLF241286H, BLF242713H, BLF242875H, BLF243142H, BLF243439H, BLF244165H, BLF242857H, BLF241855H, BLF243385H, BLF244651H, BLF242395H, BLF243179H, BLF242005H, BLF243442H, BLF244061H, BLF243397H, BLF242133H, BLF243010H, BLF243418H, BLF243435H, BLF243464H, BLF244080H, BLF240020H, BLF242060H, BLF242096H, BLF242674H, BLF242711H, BLF243068H, BLF243171H, BLF243430H, BLF243444H, BLF241170H, BLF244117H, BLF243086H, BLF243936H, BLF242691H, BLF243136H, BLF240023H, BLF242666H, BLF243941H, BLF243877H, BLF241596H, BLF242696H, BLF240265H, BLF241136H, BLF243474H, BLF240009H, BLF243059H, BLF243935H, BLF240016H, BLF241267H, BLF242876H, BLF241795H, BLF242444H, BLF243432H, BLF241869H, BLF243407H, BLF241846H, BLF242068H, BLF243808H, BLF243019H, BLF242260H, BLF243518H, BLF243506H, BLF244134H, BLF240017H, BLF242923H, BLF243089H, BLF240406H, BLF242391H, BLF242658H, BLF243096H, BLF240648H, BLF241838H, BLF241848H, BLF243495H, BLF240003H, BLF242405H, BLF242663H, BLF240032H, BLF241760H, BLF242324H, BLF242657H, BLF242707H, BLF244003H, BLF239398H, BLF240010H, BLF236242H, BLF240008H, BLF243030H, BLF243082H, BLF243479H, BLF243480H, BLF238259H, BLF238700H, BLF239843H, BLF242063H, BLF243447H, BLF240024H, BLF240547H, BLF242348H, BLF243056H, BLF243090H, BLF243105H, BLF239263H, BLF241473H, BLF242940H, BLF239773H, BLF240033H, BLF242708H, BLF243231H, BLF243667H, BLF238847H, BLF242209H, BLF240083H, BLF242680H, BLF242709H, BLF239264H, BLF242784H, BLF240503H, BLF243138H, BLF242471H, BLF243406H, BLF239866H, BLF241016H, BLF240879H, BLF241839H, BLF243034H, BLF243369H, BLF244112H, BLF243419H, BLF243708H, BLF241847H, BLF243405H, BLF243491H, BLF241851H, BLF242075H, BLF240794H, BLF241091H, BLF243424H, BLF239117H, BLF239889H, BLF242080H, BLF243976H, BLF244652H, BLF239615H, BLF242014H, BLF240857H, BLF243168H, BLF243791H, BLF240782H, BLF240830H, BLF242100H, BLF242779H, BLF243426H, BLF243449H, BLF243648H, BLF244128H, BLF244497H, BLF239864H, BLF242009H, BLF239244H, BLF239351H, BLF241853H, BLF241824H, BLF242007H, BLF242035H, BLF242204H, BLF242811H, BLF243511H, BLF233474H, BLF242026H, BLF242062H, BLF242910H, BLF243583H, BLF244009H, BLF238616H, BLF239587H, BLF240472H, BLF241836H, BLF241850H, BLF242024H, BLF242507H, BLF243373H, BLF243415H, BLF244508H, BLF239718H, BLF242021H, BLF242453H, BLF242808H, BLF243988H, BLF244500H, BLF242011H, BLF243955H, BLF244225H, BLF244573H, BLF240691H, BLF244431H, BLF242669H, BLF242817H, BLF244592H, BLF242008H, BLF238801H, BLF243255H, BLF235186H, BLF242114H, BLF242458H, BLF242877H, BLF238492H, BLF240026H, BLF239089H, BLF241043H, BLF241675H, BLF244655H, BLF243212H, BLF242249H, BLF243134H, BLF235187H, BLF236322H, BLF240612H, BLF239475H, BLF240856H, BLF241021H, BLF244471H, BLF244400H, BLF241010H, BLF243715H, BLF237913H, BLF238189H, BLF243062H, BLF244126H, BLF238047H, BLF243496H, BLF242066H, BLF239803H, BLF243857H, BLF244274H, BLF244562H, BLF236223H, BLF241307H, BLF242386H, BLF243473H, BLF243874H, BLF244381H, BLF244646H, BLF241843H, BLF244658H, BLF237433H, BLF238074H, BLF242735H, BLF235855H, BLF236051H, BLF242715H, BLF243294H, BLF243434H, BLF243274H, BLF241507H, BLF243198H, BLF243392H, BLF243505H, BLF243563H, BLF244312H, BLF241458H, BLF243451H, BLF243458H, BLF240776H, BLF244203H, BLF236843H, BLF236967H, BLF243061H, BLF237015H, BLF240254H, BLF240662H, BLF243612H, BLF241809H, BLF242334H, BLF242448H, BLF242812H, BLF244326H, BLF242901H, BLF243271H, BLF243652H, BLF244555H, BLF231669H, BLF235896H, BLF236939H, BLF238586H, BLF240895H, BLF243113H, BLF243762H, BLF241104H, BLF243525H, BLF243675H, BLF234586H, BLF238437H, BLF243388H, BLF243481H, BLF236549H, BLF239751H, BLF242896H, BLF243994H, BLF236965H, BLF243336H, BLF242639H, BLF235829H, BLF236571H, BLF241570H, BLF243423H, BLF244191H, BLF242221H, BLF244536H, BLF244159H, BLF238282H, BLF238845H, BLF238846H, BLF239749H, BLF234862H, BLF244276H, BLF235394H, BLF237489H, BLF243818H, BLF244071H, BLF235640H, BLF242889H, BLF243960H, BLF241297H, BLF239566H, BLF243687H, BLF244215H, BLF235675H, BLF240908H, BLF241314H, BLF241478H, BLF242645H, BLF243582H, BLF243906H, BLF241715H, BLF244467H, BLF233023H, BLF239304H, BLF2434… (truncated, 2884485 characters total — see the official FDA record for the full value)
Recalling firm:
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 5, 2021

System INFX-8000F

The x-ray irradiation field may shift with respect to image receiving surface displayed on the screen at some C-arm angles.

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▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
87419
Lot/product code:
Model: CAS-880A, CAS-830B
Recalling firm:
Canon Medical System, USA, INC.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 5, 2021

System INFX-8000C

The x-ray irradiation field may shift with respect to image receiving surface displayed on the screen at some C-arm angles.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
87419
Lot/product code:
Model: CAS-880A, CAS-830B
Recalling firm:
Canon Medical System, USA, INC.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 5, 2021

System INFX-8000V

The x-ray irradiation field may shift with respect to image receiving surface displayed on the screen at some C-arm angles.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
87419
Lot/product code:
Model: CAS-880A, CAS-830B
Recalling firm:
Canon Medical System, USA, INC.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 7, 2021

NM/CT 870 DR Nuclear Medicine / CT Scanners

GE Healthcare has become aware of a potential issue on 800 family NM/CT Scanners that could cause a shift in CT radiation exposure range of up to 5cm compared to the intended radiation exposure range of the planned scan under specific workflows. The issue occurs only on a hybrid whole-body continuous F3 protocol with Zoom < 1 where the scan range is set on the Smart Console. In some cases, this may also necessitate a re-scan of the patient, which would expose the patient to additional X-ray radiation.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
87811
Lot/product code:
GTIN*00840682140836
Recalling firm:
GE Healthcare, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 7, 2021

NM/CT 850 Nuclear Medicine / CT Scanners

GE Healthcare has become aware of a potential issue on 800 family NM/CT Scanners that could cause a shift in CT radiation exposure range of up to 5cm compared to the intended radiation exposure range of the planned scan under specific workflows. The issue occurs only on a hybrid whole-body continuous F3 protocol with Zoom < 1 where the scan range is set on the Smart Console. In some cases, this may also necessitate a re-scan of the patient, which would expose the patient to additional X-ray radiation.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
87811
Lot/product code:
GTIN*00840682140775
Recalling firm:
GE Healthcare, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 7, 2021

NM/CT 860 Nuclear Medicine / CT Scanners

GE Healthcare has become aware of a potential issue on 800 family NM/CT Scanners that could cause a shift in CT radiation exposure range of up to 5cm compared to the intended radiation exposure range of the planned scan under specific workflows. The issue occurs only on a hybrid whole-body continuous F3 protocol with Zoom < 1 where the scan range is set on the Smart Console. In some cases, this may also necessitate a re-scan of the patient, which would expose the patient to additional X-ray radiation.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
87811
Lot/product code:
GTIN*00840682140751
Recalling firm:
GE Healthcare, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 8, 2021

Mizuho CE IPX4, mode MOT-5602BW, 100-240, 50-60Hz, 400VA, REF 18-140-20 containing hand control Unit - Product Usage: intended to support a patient during surgical operations.

There is a potential that hand control units may cause the tabletop to slide in the opposite direction from that selected by the user. This could result in a delay in procedure.

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▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
87318
Lot/product code:
S/N (Control unit) - S/N (Operating table): 10290134 - MEC-20195-0034, 10290135 - MEC-20195-0036, 10290136 - MEC-20195-0035, 10290137 - MEC-20195-0033, 10490143 - MEC-20198-0038, 10490144 - MEC-20198-0037, 10490145 - MEC-20198-0040, 10490147 - MEC-20198-0039, 10690148 - MEC-2019Y-0054, 10690149 - MEC-20199-0049, 10690150 - MEC-2019Y-0059, 10690153 - MEC-2019Y-0058, 10690154 - MEC-20199-0046, 10690155 - MEC-2019Y-0057, 10690156 - MEC-20199-0050, 10690157 - MEC-20199-0044, 10690159 - MEC-20199-0047, 10690160 - MEC-20199-0051, 10690161 - MEC-20199-0045, 10690162 - MEC-20199-0048, 10690163 - MEC-2019Y-0053, 10790167 - MEC-2019Y-0052, 10790169 - MEC-2019Y-0056, 10790170 - MEC-2019Y-0055, 211080129 - MEC-2018Z-0029, 11080130 - MEC-2018Z-0028
Recalling firm:
Mizuho OSI
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 12, 2021

NUVASIVE FREEDOM: End Cap for PRECICE Intramedullary Limb Lengthening System Implant; Packaged End Cap 8.5/10.7mm, +0mm; Packaged End Cap 8.5/10.7mm, +5mm; Packaged End Cap 8.5/10.7mm, +10mm; Packaged End Cap 8.5/10.7mm, +15mm; Packaged End Cap 8.5/10.7mm, +20mm; Packaged End Cap 12.5mm, +0mm; Packaged End Cap 12.5mm, +5mm; Packaged End Cap 12.5mm, +10mm; Packaged End Cap 12.5mm, +15mm; Packaged End Cap 12.5mm, +20mm; 4.0 mm Locking Screw 20 mm Length; 4.0 mm Locking Screw 25 mm Length; 4.0 mm Locking Screw 30 mm Length; 4.0 mm Locking Screw 35 mm Length; 4.0 mm Locking Screw 40 mm Length; 4.0 mm Locking Screw 45 mm Length; 4.0 mm Locking Screw 50 mm Length; 4.0 mm Locking Screw 55 mm Length; 4.0 mm Locking Screw 60 mm Length; 5.0 mm Locking Screw 20 mm Length; 5.0 mm Locking Screw 25 mm Length; 5.0 mm Locking Screw 30 mm Length; 5.0 mm Locking Screw 35 mm Length; 5.0 mm Locking Screw 40 mm Length; 5.0 mm Locking Screw 45 mm Length; 5.0 mm Locking Screw 50 mm Length; 5.0 mm Locking Screw 55 mm Length; 5.0 mm Locking Screw 60 mm Length; 5.0 mm Locking Screw 65 mm Length; 5.0 mm Locking Screw 70 mm Length; 5.0 mm Locking Screw 75 mm Length; 4.0 mm Locking Screw 20 mm Length; 4.0 mm Locking Screw 25 mm Length; 4.0 mm Locking Screw 30 mm Length; 4.0 mm Locking Screw 35 mm Length; 4.0 mm Locking Screw 40 mm Length; 4.0 mm Locking Screw 45 mm Length; 4.0 mm Locking Screw 50 mm Length; 4.0 mm Locking Screw 55 mm Length; 4.0 mm Locking Screw 60 mm Length; 4.0 mm X 65 mm Locking Screw, Peg; 4.0 mm X 70 mm Locking Screw, Peg; 4.0 mm X 75 mm Locking Screw, Peg; 4.0 mm X 80 mm Locking Screw, Peg; 4.0 mm X 85 mm Locking Screw, Peg; 4.0 mm X 90 mm Locking Screw, Peg; 4.0 mm X 95 mm Locking Screw, Peg; 4.0 mm X 100 mm Locking Screw, Peg; 5.0 mm Locking Screw 20 mm Length; 5.0 mm Locking Screw 25 mm Length; 5.0 mm Locking Screw 30 mm Length; 5.0 mm Locking Screw 35 mm Length; 5.0 mm Locking Screw 40 mm Length; 5.0 mm Locking Screw 45 mm Length; 5.0 mm Locking Screw 50 mm Length; 5.0 mm Locking Screw 55 mm Length; 5.0 mm Locking Screw 60 mm Length; 5.0 mm Locking Screw 65 mm Length; 5.0 mm Locking Screw 70 mm Length; 5.0 mm Locking Screw 75 mm Length; 5.0 mm X 80 mm Locking Screw, Peg; 5.0 mm X 85 mm Locking Screw, Peg; 5.0 mm X 90 mm Locking Screw, Peg; 5.0 mm X 95 mm Locking Screw, Peg; 5.0 mm X 100 mm Locking Screw, Peg; Orthopedic intramedullary limb lengthening rod, residual limb lengthener, 14 mm diameter, 130 mm length; Orthopedic surgical instrument - for use with the intramedullary limb lengthening rod, residual limb lengthener;

Due to not having the full complement of biological assessments for all potential patients and as a result the devices are not indicated for use in individuals under the age of 18 years old.

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FDA has not published a risk classification for this recall yet.

Recall #:
87353
Lot/product code:
All Lots manufactured between April 2015 to February 2021.  NUVASIVE Freedom Product Codes:  End Caps:  CPA1-000; CPA2-000; CPA2-005; CPA2-010; CPA2-015; CPA2-020; CPA3-000; CPA3-005; CPA3-010; CPA3-015; CPA3-020;   Locking screws:  LSB4-020; LSB4-025; LSB4-030; LSB4-035; LSB4-040; LSB4-045; LSB4-050; LSB4-055; LSB4-060; LSB5-020; LSB5-025; LSB5-030; LSB5-035; LSB5-040; LSB5-045; LSB5-050; LSB5-055; LSB5-060; LSB5-065; LSB5-070; LSB5-075; LSC4-020; LSC4-025; LSC4-030; LSC4-035; LSC4-040; LSC4-045; LSC4-050; LSC4-055; LSC4-060; LSC4-065; LSC4-070; LSC4-075; LSC4-080; LSC4-085; LSC4-090; LSC4-095; LSC4-100; LSC5-020; LSC5-025; LSC5-030; LSC5-035; LSC5-040; LSC5-045; LSC5-050; LSC5-055; LSC5-060; LSC5-065; LSC5-070; LSC5-075; LSC5-080; LSC5-085; LSC5-090; LSC5-095; LSC5-100;  Limb lengthening intramedullary rod, residual limb lengthener:  R14-100A130;  Orthopedic surgical instrument - for use with the intramedullary limb lengthening rod, residual limb lengthener:  RLL1-000;  GTIN Numbers: 00812258020002; 00887517001139; 00887517001146; 00887517001153; 00887517001160; 00887517001177; 00887517001184; 00887517001191; 00887517001207; 00887517001214; 00887517001221; 00856719002763; 00856719002770; 00856719002787; 00856719002794; 00856719002800; 00856719002817; 00856719002824; 00856719002831; 00856719002848; 00856719002886; 00856719002893; 00856719002909; 00856719002916; 00856719002923; 00856719002930; 00856719002947; 00856719002954; 00856719002961; 00856719002978; 00856719002985; 00856719002992; 00812258021429; 00812258021436; 00812258021443; 00812258021450; 00812258021467; 00812258021474; 00812258021481; 00812258021498; 00812258021504; 00887517000958; 00887517000965; 00887517000972; 00887517000989; 00887517000996; 00887517001009; 00887517001016; 00887517001023; 00812258021511; 00812258021528; 00812258021535; 00812258021542; 00812258021559; 00812258021566; 00812258021573; 00812258021580; 00812258021597; 00812258021603; 00812258021610; 00812258021627; 00887517001030; 00887517001047; 00887517001054; 00887517001061; 00887517001078; 00812258024239; 00812258026479;
Recalling firm:
Nuvasive Specialized Orthopedics Inc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 12, 2021

PRECICE PLATE - Product Usage: intended for limb lengthening, open and closed fracture fixation, pseudoarthrosis, mal-unions, non-unions, or bone transport of long bones.

Due to complaints of adverse events potentially related to biological safety. The complaints included report of pain and bony abnormalities at the interface between the telescoping nail segments.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
87352
Lot/product code:
All Lots affected.  Below are: Primary DI Number(GTIN)/Product Code (REF)/Product Description: 00887517021915 LP4.5-DLF30 PRECICE Plate 4.5mm Distal Femur Plate, Left, 35mm, 0-Hole; 00887517021908 LP4.5-DLF31 PRECICE Plate 4.5mm Distal Femur Plate, Left, 35mm, 1-Hole; 00887517021892 LP4.5-DLF32 PRECICE Plate 4.5mm Distal Femur Plate, Left, 35mm, 2-Hole; 00887517021885 LP4.5-DLF3B PRECICE Plate 4.5mm Distal Femur Plate, Left, 35mm, Bump; 00887517021878 LP4.5-DLF40 PRECICE Plate 4.5mm Distal Femur Plate, Left, 45mm, 0-Hole; 00887517021861 LP4.5-DLF41 PRECICE Plate 4.5mm Distal Femur Plate, Left, 45mm, 1-Hole; 00887517021854 LP4.5-DLF42 PRECICE Plate 4.5mm Distal Femur Plate, Left, 45mm, 2-Hole; 00887517021847 LP4.5-DLF4B PRECICE Plate 4.5mm Distal Femur Plate, Left, 45mm, Bump; 00887517021830 LP4.5-DRF30 PRECICE Plate 4.5mm Distal Femur Plate, Right, 35mm, 0-Hole; 00887517021823 LP4.5-DRF31 PRECICE Plate 4.5mm Distal Femur Plate, Right, 35mm, 1-Hole; 00887517021816 LP4.5-DRF32 PRECICE Plate 4.5mm Distal Femur Plate, Right, 35mm, 2-Hole; 00887517021809 LP4.5-DRF3B PRECICE Plate 4.5mm Distal Femur Plate, Right, 35mm, Bump; 00887517021793 LP4.5-DRF40 PRECICE Plate 4.5mm Distal Femur Plate, Right, 45mm, 0-Hole; 00887517021786 LP4.5-DRF41 PRECICE Plate 4.5mm Distal Femur Plate, Right, 45mm, 1-Hole; 00887517021779 LP4.5-DRF42 PRECICE Plate 4.5mm Distal Femur Plate, Right, 45mm, 2-Hole; 00887517021762 LP4.5-DRF4B PRECICE Plate 4.5mm Distal Femur Plate, Right, 45mm, Bump; 00887517021755 LP4.5-MLT30 PRECICE Plate 4.5mm Posteromedial Proximal Tibia Plate, Left, 35mm, 0-Hole; 00887517021748 LP4.5-MLT31 PRECICE Plate 4.5mm Posteromedial Proximal Tibia Plate, Left, 35mm, 1-Hole; 00887517021731 LP4.5-MLT32 PRECICE Plate 4.5mm Posteromedial Proximal Tibia Plate, Left, 35mm, 2-Hole; 00887517021724 LP4.5-MLT3B PRECICE Plate 4.5mm Posteromedial Proximal Tibia Plate, Left, 35mm, Bump; 00887517021717 LP4.5-MLT40 PRECICE Plate 4.5mm Posteromedial Proximal Tibia Plate, Left, 45mm, 0-Hole; 00887517021700 LP4.5-MLT41 PRECICE Plate 4.5mm Posteromedial Proximal Tibia Plate, Left, 45mm, 1-Hole; 00887517021694 LP4.5-MLT42 PRECICE Plate 4.5mm Posteromedial Proximal Tibia Plate, Left, 45mm, 2-Hole; 00887517021687 LP4.5-MLT4B PRECICE Plate 4.5mm Posteromedial Proximal Tibia Plate, Left, 45mm, Bump; 00887517021670 LP4.5-MRT30 PRECICE Plate 4.5mm Posteromedial Proximal Tibia Plate, Right, 35mm, 0-Hole; 00887517021663 LP4.5-MRT31 PRECICE Plate 4.5mm Posteromedial Proximal Tibia Plate, Right, 35mm, 1-Hole; 00887517021656 LP4.5-MRT32 PRECICE Plate 4.5mm Posteromedial Proximal Tibia Plate, Right, 35mm, 2-Hole; 00887517021649 LP4.5-MRT3B PRECICE Plate 4.5mm Posteromedial Proximal Tibia Plate, Right, 35mm, Bump; 00887517021632 LP4.5-MRT40 PRECICE Plate 4.5mm Posteromedial Proximal Tibia Plate, Right, 45mm, 0-Hole; 00887517021625 LP4.5-MRT41 PRECICE Plate 4.5mm Posteromedial Proximal Tibia Plate, Right, 45mm, 1-Hole; 00887517021618 LP4.5-MRT42 PRECICE Plate 4.5mm Posteromedial Proximal Tibia Plate, Right, 45mm, 2-Hole; 00887517021601 LP4.5-MRT4B PRECICE Plate 4.5mm Posteromedial Proximal Tibia Plate, Right, 45mm, Bump; 00887517021595 LP4.5-PLF30 PRECICE Plate 4.5mm Proximal Femur Plate, Left, 35mm, 0-Hole; 00887517021588 LP4.5-PLF31 PRECICE Plate 4.5mm Proximal Femur Plate, Left, 35mm, 1-Hole; 00887517021571 LP4.5-PLF32 PRECICE Plate 4.5mm Proximal Femur Plate, Left, 35mm, 2-Hole; 00887517021564 LP4.5-PLF3B PRECICE Plate 4.5mm Proximal Femur Plate, Left, 35mm, Bump; 00887517021557 LP4.5-PLF40 PRECICE Plate 4.5mm Proximal Femur Plate, Left, 45mm, 0-Hole; 00887517021540 LP4.5-PLF41 PRECICE Plate 4.5mm Proximal Femur Plate, Left, 45mm, 1-Hole; 00887517021533 LP4.5-PLF42 PRECICE Plate 4.5mm Proximal Femur Plate, Left, 45mm, 2-Hole; 00887517021526 LP4.5-PLF4B PRECICE Plate 4.5mm Proximal Femur Plate, Left, 45mm, Bump; 00887517021519 LP4.5-PLT30 PRECICE Plate 4.5mm Proximal Tibia Plate, Left, 35mm, 0-Hole; 00887517021502 LP4.5-PLT31 PRECICE Plate 4.5mm Proximal Tibia Plate, Left, 35mm, 1-Hole; 00887517021496 LP4.5-PLT32 PRECICE Plate 4.5mm Proximal Tibia Plate, Left, 35mm, 2-Hole; 00887517021489 LP4.5-PLT3B PRECICE Plate 4.5mm Proximal Tibia Plate, Left, 35mm, Bump; 00887517021472 LP4.5-PLT40 PRECICE Plate 4.5mm Proximal Tibia Plate, Left, 45mm, 0-Hole; 00887517021465 LP4.5-PLT41 PRECICE Plate 4.5mm Proximal Tibia Plate, Left, 45mm, 1-Hole; 00887517021458 LP4.5-PLT42 PRECICE Plate 4.5mm Proximal Tibia Plate, Left, 45mm, 2-Hole; 00887517021441 LP4.5-PLT4B PRECICE Plate 4.5mm Proximal Tibia Plate, Left, 45mm, Bump; 00887517021434 LP4.5-PRF30 PRECICE Plate 4.5mm Proximal Femur Plate, Right, 35mm, 0-Hole; 00887517021427 LP4.5-PRF31 PRECICE Plate 4.5mm Proximal Femur Plate, Right, 35mm, 1-Hole; 00887517021410 LP4.5-PRF32 PRECICE Plate 4.5mm Proximal Femur Plate, Right, 35mm, 2-Hole; 00887517021403 LP4.5-PRF3B PRECICE Plate 4.5mm Proximal Femur Plate, Right, 35mm, Bump; 00887517021397 LP4.5-PRF40 PRECICE Plate 4.5mm Proximal Femur Plate, Right, 45mm, 0-Hole; 0… (truncated, 6067 characters total — see the official FDA record for the full value)
Recalling firm:
Nuvasive Specialized Orthopedics Inc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 12, 2021

Precice Bone Transport - Product Usage: intended for limb lengthening, open and closed fracture fixation, pseudoarthrosis, mal-unions, non-unions, or bone transport of long bones.

Due to complaints of adverse events potentially related to biological safety. The complaints included report of pain and bony abnormalities at the interface between the telescoping nail segments.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
87352
Lot/product code:
All Lots affected.  Below are: Primary DI Number(GTIN)/Product Code (REF)/Product Description: 887517981370 BT10-100C360-5 Antegrade Tibia 10¿ Bend, 10.0mm x 360mm, 5/10cm ST; 887517981554 BT10-10A360-5 Retrograde Femur 10¿ Bend, 10.0mm x 360mm, 5/10cm ST; 887517981547 BT10-10A360-7 Retrograde Femur 10¿ Bend, 10.0mm x 360mm, 7/10cm ST; 887517981530 BT10-10A380-5 Retrograde Femur 10¿ Bend, 10.0mm x 380mm, 5/10cm ST; 887517981523 BT10-10A380-7 Retrograde Femur 10¿ Bend, 10.0mm x 380mm, 7/10cm ST; 887517981516 BT10-10A400-5 Retrograde Femur 10¿ Bend, 10.0mm x 400mm, 5/10cm ST; 887517981509 BT10-10A400-7 Retrograde Femur 10¿ Bend, 10.0mm x 400mm, 7/10cm ST; 887517981493 BT10-10B360-5 Antegrade Femur Piriformis Straight, 10.0mm x 360mm, 5/10cm ST; 887517981486 BT10-10B360-7 Antegrade Femur Piriformis Straight, 10.0mm x 360mm, 7/10cm ST; 887517981479 BT10-10B380-5 Antegrade Femur Piriformis Straight, 10.0mm x 380mm, 5/10cm ST; 887517981462 BT10-10B380-7 Antegrade Femur Piriformis Straight, 10.0mm x 380mm, 7/10cm ST; 887517981455 BT10-10B400-5 Antegrade Femur Piriformis Straight, 10.0mm x 400mm, 5/10cm ST; 887517981448 BT10-10B400-7 Antegrade Femur Piriformis Straight, 10.0mm x 400mm, 7/10cm ST; 887517981431 BT10-10BT360-5 Antegrade Femur Piriformis Straight, 10.0mm x 360mm, 5/10cm ST; 887517981424 BT10-10BT360-7 Antegrade Femur Piriformis Straight, 10.0mm x 360mm, 7/10cm ST; 887517981417 BT10-10BT380-5 Antegrade Femur Piriformis Straight, 10.0mm x 380mm, 5/10cm ST; 887517981400 BT10-10BT380-7 Antegrade Femur Piriformis Straight, 10.0mm x 380mm, 7/10cm ST; 887517981394 BT10-10BT400-5 Antegrade Femur Piriformis Straight, 10.0mm x 400mm, 5/10cm ST; 887517981387 BT10-10BT400-7 Antegrade Femur Piriformis Straight, 10.0mm x 400mm, 7/10cm ST; 887517981363 BT10-10C360-7 Antegrade Tibia 10¿ Bend, 10.0mm x 360mm, 7/10cm ST; 887517981356 BT10-10C380-5 Antegrade Tibia 10¿ Bend, 10.0mm x 380mm, 5/10cm ST; 887517981349 BT10-10C380-7 Antegrade Tibia 10¿ Bend, 10.0mm x 380mm, 7/10cm ST; 887517981332 BT10-10C400-5 Antegrade Tibia 10¿ Bend, 10.0mm x 400mm, 5/10cm ST; 887517981325 BT10-10C400-7 Antegrade Tibia 10¿ Bend, 10.0mm x 400mm, 7/10cm ST; 887517981318 BT10-10D360-5 Antegrade Femur Trochanter 10¿ Bend, 10.0mm x 360mm, 5/10cm ST; 887517981301 BT10-10D360-7 Antegrade Femur Trochanter 10¿ Bend, 10.0mm x 360mm, 7/10cm ST; 887517981295 BT10-10D380-5 Antegrade Femur Trochanter 10¿ Bend, 10.0mm x 380mm, 5/10cm ST; 887517981288 BT10-10D380-7 Antegrade Femur Trochanter 10¿ Bend, 10.0mm x 380mm, 7/10cm ST; 887517981271 BT10-10D400-5 Antegrade Femur Trochanter 10¿ Bend, 10.0mm x 400mm, 5/10cm ST; 887517981264 BT10-10D400-7 Antegrade Femur Trochanter 10¿ Bend, 10.0mm x 400mm, 7/10cm ST; 887517981257 BT10-10DT360-5 Antegrade Femur Trochanter 10¿ Bend, 10.0mm x 360mm, 5/10cm ST; 887517981240 BT10-10DT360-7 Antegrade Femur Trochanter 10¿ Bend, 10.0mm x 360mm, 7/10cm ST; 887517981233 BT10-10DT380-5 Antegrade Femur Trochanter 10¿ Bend, 10.0mm x 380mm, 5/10cm ST; 887517981226 BT10-10DT380-7 Antegrade Femur Trochanter 10¿ Bend, 10.0mm x 380mm, 7/10cm ST; 887517981219 BT10-10DT400-5 Antegrade Femur Trochanter 10¿ Bend, 10.0mm x 400mm, 5/10cm ST; 887517981202 BT10-10DT400-7 Antegrade Femur Trochanter 10¿ Bend, 10.0mm x 400mm, 7/10cm ST; 887517981196 BT10-10E360-5 Retrograde Femur Straight, 10.0mm x 360mm, 5/10cm ST; 887517981189 BT10-10E360-7 Retrograde Femur Straight, 10.0mm x 360mm, 7/10cm ST; 887517981172 BT10-10E380-5 Retrograde Femur Straight, 10.0mm x 380mm, 5/10cm ST; 887517981165 BT10-10E380-7 Retrograde Femur Straight, 10.0mm x 380mm, 7/10cm ST; 887517981158 BT10-10E400-5 Retrograde Femur Straight, 10.0mm x 400mm, 5/10cm ST; 887517981141 BT10-10E400-7 Retrograde Femur Straight, 10.0mm x 400mm, 7/10cm ST; 887517981134 BT10-10SA360-5 Retrograde Femur 5¿ Bend Three Holes, 10.0mm x 360mm, 5/10cm ST; 887517981127 BT10-10SA360-7 Retrograde Femur 5¿ Bend Three Holes, 10.0mm x 360mm, 7/10cm ST; 887517981110 BT10-10SA380-5 Retrograde Femur 5¿ Bend Three Holes, 10.0mm x 380mm, 5/10cm ST; 887517981103 BT10-10SA380-7 Retrograde Femur 5¿ Bend Three Holes, 10.0mm x 380mm, 7/10cm ST; 887517981097 BT10-10SA400-5 Retrograde Femur 5¿ Bend Three Holes, 10.0mm x 400mm, 5/10cm ST; 887517981080 BT10-10SA400-7 Retrograde Femur 5¿ Bend Three Holes, 10.0mm x 400mm, 7/10cm ST; 887517981073 BT10-10SB360-5 Recon Antegrade Femur Piriformis Straight, 10.0mm x 360mm, 5/10cm ST; 887517981066 BT10-10SB360-7 Recon Antegrade Femur Piriformis Straight, 10.0mm x 360mm, 7/10cm ST; 887517981059 BT10-10SB380-5 Recon Antegrade Femur Piriformis Straight, 10.0mm x 380mm, 5/10cm ST; 887517981042 BT10-10SB380-7 Recon Antegrade Femur Piriformis Straight, 10.0mm x 380mm, 7/10cm ST; 887517981035 BT10-10SB400-5 Recon Antegrade Femur Piriformis Straight, 10.0mm x 400mm, 5/10cm ST; 887517981028 BT10-10SB400-7 Recon Antegrade Femur Piriformis Straight, 10.0mm x 400mm, 7/10cm ST; 887517981011 BT10-10SD360-5 Recon Antegrade Femur Trochanter 10¿ Bend, 10.0mm x 360mm, 5/10cm ST; 887517… (truncated, 49623 characters total — see the official FDA record for the full value)
Recalling firm:
Nuvasive Specialized Orthopedics Inc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 12, 2021

NUVASIVE PRECICE UNYTE System (Humerus and Tibia): PRECICE Trauma Nail System/PRECICE Unyte-Humerus Orthopedic trauma intramedullary rod, humerus, 8.5 mm diameter, 165 mm length; Orthopedic trauma intramedullary rod, humerus, 8.5 mm diameter, 180 mm length; Orthopedic trauma intramedullary rod, humerus, 8.5 mm diameter, 195 mm length; Orthopedic trauma intramedullary rod, humerus, 8.5 mm diameter, 210 mm length; Orthopedic trauma intramedullary rod, humerus, 8.5 mm diameter, 225 mm length; Orthopedic trauma intramedullary rod, humerus, 8.5 mm diameter, 240 mm length; Orthopedic trauma intramedullary rod, humerus, 8.5 mm diameter, 255 mm length; Orthopedic trauma intramedullary rod, humerus, 8.5 mm diameter, 270 mm length; Orthopedic trauma intramedullary rod, humerus, 8.5 mm diameter, 285 mm length; Orthopedic trauma intramedullary rod, humerus, 8.5 mm diameter, 300 mm length; End Cap for PRECICE Trauma Intramedullary Nail System Implant (humeral nail, 0mm); End Cap for PRECICE Trauma Intramedullary Nail System Implant (humeral nail, 2mm); End Cap for PRECICE Trauma Intramedullary Nail System Implant (humeral nail, 5mm); End Cap for PRECICE Trauma Intramedullary Nail System Implant (humeral nail, 10mm); End Cap for PRECICE Trauma Intramedullary Nail System Implant (humeral nail, 15mm); End Cap for PRECICE Trauma Intramedullary Nail System Implant (humeral nail, 0mm); End Cap for PRECICE Trauma Intramedullary Nail System Implant (humeral nail, 2mm); End Cap for PRECICE Trauma Intramedullary Nail System Implant (humeral nail, 5mm); End Cap for PRECICE Trauma Intramedullary Nail System Implant (humeral nail, 10mm); End Cap for PRECICE Trauma Intramedullary Nail System Implant (humeral nail, 15mm); 3.5 mm Locking Screw, 20 mm Length; 3.5 mm Locking Screw 25 mm Length; 3.5 mm Locking Screw 30 mm Length; 3.5 mm Locking Screw 35 mm Length; 3.5 mm Locking Screw 40 mm Length; 3.5 mm Locking Screw 45 mm Length; 3.5 mm Locking Screw 50 mm Length; 3.5 mm Locking Screw 55 mm Length; 3.5 mm Locking Screw 60 mm Length; Locking Screw, 3.5x65mm; Locking Screw, 3.5x70mm; Locking Screw, 3.5x75mm; 5.0 mm Locking Screw 20 mm Length; 5.0 mm Locking Screw 25 mm Length; 5.0 mm Locking Screw 30 mm Length; 5.0 mm Locking Screw 35 mm Length; 5.0 mm Locking Screw 40 mm Length; 5.0 mm Locking Screw 45 mm Length; 5.0 mm Locking Screw 50 mm Length; 5.0 mm Locking Screw 55 mm Length; 5.0 mm Locking Screw 60 mm Length; 5.0 mm Locking Screw 65 mm Length; 5.0 mm Locking Screw 70 mm Length; 5.0 mm Locking Screw 75 mm Length; 5.0 mm Locking Screw 20 mm Length; 5.0 mm Locking Screw 25 mm Length; 5.0 mm Locking Screw 30 mm Length; 5.0 mm Locking Screw 35 mm Length; 5.0 mm Locking Screw 40 mm Length; 5.0 mm Locking Screw 45 mm Length; 5.0 mm Locking Screw 50 mm Length; 5.0 mm Locking Screw 55 mm Length; 5.0 mm Locking Screw 60 mm Length; 5.0 mm Locking Screw 65 mm Length; 5.0 mm Locking Screw 70 mm Length; 5.0 mm Locking Screw 75 mm Length; 5.0 mm X 80 mm Locking Screw, Peg; 5.0 mm X 85 mm Locking Screw, Peg; 5.0 mm X 90 mm Locking Screw, Peg; 5.0 mm X 95 mm Locking Screw, Peg; 5.0 mm X 100 mm Locking Screw, Peg; PRECICE Trauma Nail System/Precice Unyte-Tibia Orthopedic trauma intramedullary rod, antegrade tibia 10 degree bend, 11.5 mm diameter, 240 mm length; Orthopedic trauma intramedullary rod, antegrade tibia 10 degree bend, 11.5 mm diameter, 255 mm length; Orthopedic trauma intramedullary rod, antegrade tibia 10 degree bend, 11.5 mm diameter, 270 mm length; Orthopedic trauma intramedullary rod, antegrade tibia 10 degree bend, 11.5 mm diameter, 285 mm length; Orthopedic trauma intramedullary rod, antegrade tibia 10 degree bend, 11.5 mm diameter, 300 mm length; Orthopedic trauma intramedullary rod, antegrade tibia 10 degree bend, 11.5 mm diameter, 315 mm length; Orthopedic trauma intramedullary rod, antegrade tibia 10 degree bend, 11.5 mm diameter, 330 mm length; Orthopedic trauma intra

Due to not having the full complement of biological assessments for all potential patients and as a result the devices are not indicated for use in individuals under the age of 18 years old.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
87353
Lot/product code:
All Lots manufactured between April 2015 to February 2021.  PRECICE Unyte Product Codes (for Humerus):   Trauma intramedullary rod, humerus, 8.5 mm diameter:  CDH8.5-20L165; CDH8.5-20L180; CDH8.5-30L195; CDH8.5-50L210; CDH8.5-50M225; CDH8.5-50M240; CDH8.5-80M255; CDH8.5-80M270; CDH8.5-80M285; CDH8.5-80M300;    end cap for trauma intramedullary humeral nail:  HEC1-000; HEC2-000; HEC3-000; HEC4-000; HEC5-000;     Locking screws:  LSB3-020; LSB3-025; LSB3-030; LSB3-035; LSB3-040; LSB3-045; LSB3-050; LSB3-055; LSB3-060; LSB3-065; LSB3-070; LSB3-075; LSB5-020; LSB5-025; LSB5-030; LSB5-035; LSB5-040; LSB5-045; LSB5-050; LSB5-055; LSB5-060; LSB5-065; LSB5-070; LSB5-075; LSC5-020; LSC5-025; LSC5-030; LSC5-035; LSC5-040; LSC5-045; LSC5-050; LSC5-055; LSC5-060; LSC5-065; LSC5-070; LSC5-075; LSC5-080; LSC5-085; LSC5-090; LSC5-095; LSC5-100.  GTIN Number (for Humerus): 00812258022730; 00812258022747; 00812258022754; 00812258022761; 00812258022778; 00812258022785; 00812258022792; 00812258022808; 00812258022815; 00812258022822; 00812258028121; 00812258028138; 00812258028145; 00812258028152; 00812258028169; 00812258021337; 00812258021344; 00812258021351; 00812258021368; 00812258021375; 00812258021382; 00812258021399; 00812258021405; 00812258021412; 00887517936233; 00887517936240; 00887517936257; 00856719002886; 00856719002893; 00856719002909; 00856719002916; 00856719002923; 00856719002930; 00856719002947; 00856719002954; 00856719002961; 00856719002978; 00856719002985; 00856719002992; 00812258021511; 00812258021528; 00812258021535; 00812258021542; 00812258021559; 00812258021566; 00812258021573; 00812258021580; 00812258021597; 00812258021603; 00812258021610; 00812258021627; 00887517001030; 00887517001047; 00887517001054; 00887517001061; 00887517001078;  Precice Unyte Product Codes (for Tibia):   trauma intramedullary rod, 11.5 mm diameter:  CDT11.5-30T240; CDT11.5-30T255; CDT11.5-30T270; CDT11.5-30T285; CDT11.5-30T300; CDT11.5-30T315; CDT11.5-30T330; CDT11.5-30T345; CDT11.5-30T360; CDT11.5-30T375; CDT11.5C-30T240; CDT11.5C-30T255; CDT11.5C-30T270; CDT11.5C-30T285; CDT11.5C-30T300; CDT11.5C-30T315; CDT11.5C-30T330; CDT11.5C-30T345; CDT11.5C-30T360; CDT11.5C-30T375;   trauma intramedullary rod, 12.5 mm diameter:  CDT12.5-30T240; CDT12.5-30T255; CDT12.5-30T270; CDT12.5-30T285; CDT12.5-30T300; CDT12.5-30T315; CDT12.5-30T330; CDT12.5-30T345; CDT12.5-30T360; CDT12.5-30T375; CDT12.5C-30T240; CDT12.5C-30T255; CDT12.5C-30T270; CDT12.5C-30T285; CDT12.5C-30T300; CDT12.5C-30T315; CDT12.5C-30T330; CDT12.5C-30T345; CDT12.5C-30T360; CDT12.5C-30T375;    end cap for trauma intramedullary nail:  TEC1-000; TEC1-005; TEC1-010; TEC1-015; TEC1-020;  Locking screws:   TSA4.5-020; TSA4.5-025; TSA4.5-030; TSA4.5-035; TSA4.5-040; TSA4.5-045; TSA4.5-050; TSA4.5-055; TSA4.5-060; TSA4.5-065; TSA4.5-070; TSA4.5-075; TSA4-020; TSA4-022.5; TSA4-025; TSA4-027.5; TSA4-030; TSA4-032.5; TSA4-035; TSA4-037.5; TSA4-040; TSA4-042.5; TSA4-045; TSA4-047.5; TSA4-050; TSA4-055; TSA4-060; TSA4-065; TSA4-070; TSA4-075; TSA4-080; TSA4-085; TSA4-090; TSA4-095; TSA4-100; TSA4-100; TSA5-020; TSA5-020; TSA5-022.5; TSA5-022.5; TSA5-025; TSA5-025; TSA5-027.5; TSA5-027.5; TSA5-030; TSA5-030; TSA5-032.5; TSA5-032.5; TSA5-035; TSA5-035; TSA5-037.5; TSA5-037.5; TSA5-040; TSA5-040; TSA5-042.5; TSA5-042.5; TSA5-045; TSA5-045; TSA5-047.5; TSA5-047.5; TSA5-050; TSA5-050; TSA5-052.5; TSA5-055; TSA5-055; TSA5-057.5; TSA5-060; TSA5-060; TSA5-062.5; TSA5-065; TSA5-065; TSA5-067.5; TSA5-070; TSA5-070; TSA5-072.5; TSA5-075; TSA5-075; TSA5-080; TSA5-080; TSA5-085; TSA5-085; TSA5-090; TSA5-090; TSA5-095; TSA5-095; TSA5-100; TSA5-100; TSA5-105; TSA5-105; TSA5-110; TSA5-110.   GTIN Number (for Tibia): 00812258027322; 00812258027339; 00812258027346; 00812258027353; 00812258027360; 00812258027377; 00812258027384; 00812258027391; 00812258027407; 00812258027414; 00812258027421; 00812258027438; 00812258027445; 00812258027452; 00812258027469; 00812258027476; 00812258027483; 00812258027490; 00812258027506; 00812258027513; 00812258027520; 00812258027537; 00812258027544; 00812258027551; 00812258027568; 00812258027575; 00812258027582; 00812258027599; 00812258027605; 00812258027612; 00812258027629; 00812258027636; 00812258027643; 00812258027650; 00812258027667; 00812258027674; 00812258027681; 00812258027698; 00812258027704; 00812258027711; 00812258028039; 00812258028046; 00812258028053; 00812258028060; 00812258028077; 00887517936011; 00887517936028; 00887517936035; 00887517936042; 00887517936059; 00887517936066; 00887517936073; 00887517936080; 00887517936097; 00887517936202; 00887517936219; 00887517936226; 00887517000033; 00887517000040; 00887517000057; 00887517000064; 00887517000071; 00887517000088; 00887517000095; 00887517000101; 00887517000118; 00887517000125; 00887517000132; 00887517000149; 00887517000156; 00887517000163; 00887517000170; 00887517000187; 00887517000194; 00887517000200; 00887517000217; 00887517000224; 00887517000231; 00887517000248; 00887517000255; 00887517000255;… (truncated, 9699 characters total — see the official FDA record for the full value)
Recalling firm:
Nuvasive Specialized Orthopedics Inc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 12, 2021

Valiant Navion Thoracic Stent Graft System. For endovascular repair of lesions in the descending thoracic aorta (DTA).

Due to the presence of type IIIb endoleaks, stent fractures, and stent ring enlargement.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
87379
Lot/product code:
Model Number (REF): VNMC2020C94TE VNMC2020C94TJ VNMC2020C94TU VNMC2222C180TE VNMC2222C180TJ VNMC2222C180TU VNMC2222C94TE VNMC2222C94TJ VNMC2222C94TU VNMC2520C186TE VNMC2520C186TJ VNMC2520C186TU VNMC2525C180TE VNMC2525C180TJ VNMC2525C180TU VNMC2525C94TE VNMC2525C94TJ VNMC2525C94TU VNMC2822C207TE VNMC2822C207TJ VNMC2822C207TU VNMC2828C182TE VNMC2828C182TJ VNMC2828C182TU VNMC2828C90TE VNMC2828C90TJ VNMC2828C90TU VNMC3125C207TE VNMC3125C207TJ VNMC3125C207TU VNMC3131C182TE VNMC3131C182TJ VNMC3131C182TU VNMC3131C223TE VNMC3131C223TJ VNMC3131C223TU VNMC3131C90TE VNMC3131C90TJ VNMC3131C90TU VNMC3428C207TE VNMC3428C207TJ VNMC3428C207TU VNMC3434C182TE VNMC3434C182TJ VNMC3434C182TU VNMC3434C223TE VNMC3434C223TJ VNMC3434C223TU VNMC3434C52TE VNMC3434C52TJ VNMC3434C52TU VNMC3434C90TE VNMC3434C90TJ VNMC3434C90TU VNMC3731C207TE VNMC3731C207TJ VNMC3731C207TU VNMC3737C182TE VNMC3737C182TJ VNMC3737C182TU VNMC3737C223TE VNMC3737C223TJ VNMC3737C223TU VNMC3737C52TE VNMC3737C52TJ VNMC3737C52TU VNMC3737C90TE VNMC3737C90TJ VNMC3737C90TU VNMC4034C200TE VNMC4034C200TJ VNMC4034C200TU VNMC4040C175TE VNMC4040C175TJ VNMC4040C175TU VNMC4040C218TE VNMC4040C218TJ VNMC4040C218TU VNMC4040C55TE VNMC4040C55TJ VNMC4040C55TU VNMC4040C95TE VNMC4040C95TJ VNMC4040C95TU VNMC4337C200TE VNMC4337C200TJ VNMC4337C200TU VNMC4343C175TE VNMC4343C175TJ VNMC4343C175TU VNMC4343C218TE VNMC4343C218TJ VNMC4343C218TU VNMC4343C55TE VNMC4343C55TJ VNMC4343C55TU VNMC4343C95TE VNMC4343C95TJ VNMC4343C95TU VNMC4640C200TE VNMC4640C200TJ VNMC4640C200TU VNMC4646C175TE VNMC4646C175TJ VNMC4646C175TU VNMC4646C218TE VNMC4646C218TJ VNMC4646C218TU VNMC4646C55TE VNMC4646C55TJ VNMC4646C55TU VNMC4646C95TE VNMC4646C95TJ VNMC4646C95TU VNMF2020C96TE VNMF2020C96TU VNMF2222C185TE VNMF2222C185TU VNMF2222C96TE VNMF2222C96TJ VNMF2222C96TU VNMF2520C185TE VNMF2520C185TJ VNMF2520C185TU VNMF2525C185TE VNMF2525C185TJ VNMF2525C185TU VNMF2525C96TE VNMF2525C96TJ VNMF2525C96TU VNMF2822C173TE VNMF2822C173TJ VNMF2822C173TU VNMF2828C174TE VNMF2828C174TJ VNMF2828C174TU VNMF2828C97TE VNMF2828C97TJ VNMF2828C97TU VNMF3125C173TE VNMF3125C173TJ VNMF3125C173TU VNMF3131C174TE VNMF3131C174TJ VNMF3131C174TU VNMF3131C229TE VNMF3131C229TJ VNMF3131C229TU VNMF3131C97TE VNMF3131C97TJ VNMF3131C97TU VNMF3428C173TE VNMF3428C173TJ VNMF3428C173TU VNMF3434C174TE VNMF3434C174TJ VNMF3434C174TU VNMF3434C229TE VNMF3434C229TJ VNMF3434C229TU VNMF3434C59TE VNMF3434C59TJ VNMF3434C59TU VNMF3434C97TE VNMF3434C97TJ VNMF3434C97TU VNMF3731C173TE VNMF3731C173TJ VNMF3731C173TU VNMF3737C174TE VNMF3737C174TJ VNMF3737C174TU VNMF3737C229TE VNMF3737C229TJ VNMF3737C229TU VNMF3737C59TE VNMF3737C59TJ VNMF3737C59TU VNMF3737C97TE VNMF3737C97TJ VNMF3737C97TU VNMF4034C185TE VNMF4034C185TJ VNMF4034C185TU VNMF4040C103TE VNMF4040C103TJ VNMF4040C103TU VNMF4040C183TE VNMF4040C183TJ VNMF4040C183TU VNMF4040C223TE VNMF4040C223TJ VNMF4040C223TU VNMF4040C62TE VNMF4040C62TJ VNMF4040C62TU VNMF4337C185TE VNMF4337C185TJ VNMF4337C185TU VNMF4343C103TE VNMF4343C103TJ VNMF4343C103TU VNMF4343C183TE VNMF4343C183TJ VNMF4343C183TU VNMF4343C223TE VNMF4343C223TJ VNMF4343C223TU VNMF4343C62TE VNMF4343C62TJ VNMF4343C62TU VNMF4640C185TE VNMF4640C185TJ VNMF4640C185TU VNMF4646C103TE VNMF4646C103TJ VNMF4646C103TU VNMF4646C183TE VNMF4646C183TJ VNMF4646C183TU VNMF4646C223TE VNMF4646C223TJ VNMF4646C223TU VNMF4646C62TE VNMF4646C62TJ VNMF4646C62TU  GTIN: 00763000100520 00763000100537 00763000100544 00763000100551 00763000100568 00763000100575 00763000100582 00763000100599 00763000100605 00763000100612 00763000100629 00763000100636 00763000100643 00763000100650 00763000100667 00763000100674 00763000100681 00763000100698 00763000100704 00763000100711 00763000100728 00763000100735 00763000100742 00763000100759 00763000100766 00763000100773 00763000100780 00763000100797 00763000100803 00763000100810 00763000100827 00763000100834 00763000100841 00763000100858 00763000100865 00763000100872 00763000100889 00763000100896 00763000100902 00763000100919 00763000100926 00763000100933 00763000100940 00763000100957 00763000100964 00763000100971 00763000100988 00763000100995 00763000101008 00763000101015 00763000101022 00763000101039 00763000101046 00763000101053 00763000101060 00763000101077 00763000101084 00763000101091 00763000101107 00763000101114 00763000101121 00763000101138 00763000101145 00763000101152 00763000101169 00763000101176 00763000101183 00763000101190 00763000101206 00763000101213 00763000101220 00763000101237 00763000101244 00763000101251 00763000101268 00763000101275 00763000112790 00763000112806 00763000112813 00763000112820 00763000112837 00763000112844 00763000112851 00763000112868 00763000112875 00763000112882 00763000112899 00763000112905 00763000112912 00763000112929 00763000112936 00763000112943 00763000112950 00763000112967 00763000112974 00763000112981 00763000112998 00763000113001 00763000113018 00763000113025 00763000113032 00763000113049 00763000113056 00763000113063 00763000113070 00763000113087 00763000113094 00763000113100 00763000113117 00763000113124 0076300011313… (truncated, 343298 characters total — see the official FDA record for the full value)
Recalling firm:
Medtronic Vascular, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 12, 2021

PRECICE STRYDE - Product Usage: intended for limb lengthening, open and closed fracture fixation, pseudoarthrosis, mal-unions, non-unions, or bone transport of long bones.

Due to complaints of adverse events potentially related to biological safety. The complaints included report of pain and bony abnormalities at the interface between the telescoping nail segments.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
87352
Lot/product code:
All Lots affected.  Below are: Primary DI Number(GTIN)/Product Code (REF)/Product Description: -887517981370 BT10-100C360-5 Antegrade Tibia 10¿ Bend, 10.0mm x 360mm, 5/10cm ST; 887517981554 BT10-10A360-5 Retrograde Femur 10¿ Bend, 10.0mm x 360mm, 5/10cm ST; 887517981547 BT10-10A360-7 Retrograde Femur 10¿ Bend, 10.0mm x 360mm, 7/10cm ST; 887517981530 BT10-10A380-5 Retrograde Femur 10¿ Bend, 10.0mm x 380mm, 5/10cm ST; 887517981523 BT10-10A380-7 Retrograde Femur 10¿ Bend, 10.0mm x 380mm, 7/10cm ST; 887517981516 BT10-10A400-5 Retrograde Femur 10¿ Bend, 10.0mm x 400mm, 5/10cm ST; 887517981509 BT10-10A400-7 Retrograde Femur 10¿ Bend, 10.0mm x 400mm, 7/10cm ST; 887517981493 BT10-10B360-5 Antegrade Femur Piriformis Straight, 10.0mm x 360mm, 5/10cm ST; 887517981486 BT10-10B360-7 Antegrade Femur Piriformis Straight, 10.0mm x 360mm, 7/10cm ST; 887517981479 BT10-10B380-5 Antegrade Femur Piriformis Straight, 10.0mm x 380mm, 5/10cm ST; 887517981462 BT10-10B380-7 Antegrade Femur Piriformis Straight, 10.0mm x 380mm, 7/10cm ST; 887517981455 BT10-10B400-5 Antegrade Femur Piriformis Straight, 10.0mm x 400mm, 5/10cm ST; 887517981448 BT10-10B400-7 Antegrade Femur Piriformis Straight, 10.0mm x 400mm, 7/10cm ST; 887517981431 BT10-10BT360-5 Antegrade Femur Piriformis Straight, 10.0mm x 360mm, 5/10cm ST; 887517981424 BT10-10BT360-7 Antegrade Femur Piriformis Straight, 10.0mm x 360mm, 7/10cm ST; 887517981417 BT10-10BT380-5 Antegrade Femur Piriformis Straight, 10.0mm x 380mm, 5/10cm ST; 887517981400 BT10-10BT380-7 Antegrade Femur Piriformis Straight, 10.0mm x 380mm, 7/10cm ST; 887517981394 BT10-10BT400-5 Antegrade Femur Piriformis Straight, 10.0mm x 400mm, 5/10cm ST; 887517981387 BT10-10BT400-7 Antegrade Femur Piriformis Straight, 10.0mm x 400mm, 7/10cm ST; 887517981363 BT10-10C360-7 Antegrade Tibia 10¿ Bend, 10.0mm x 360mm, 7/10cm ST; 887517981356 BT10-10C380-5 Antegrade Tibia 10¿ Bend, 10.0mm x 380mm, 5/10cm ST; 887517981349 BT10-10C380-7 Antegrade Tibia 10¿ Bend, 10.0mm x 380mm, 7/10cm ST; 887517981332 BT10-10C400-5 Antegrade Tibia 10¿ Bend, 10.0mm x 400mm, 5/10cm ST; 887517981325 BT10-10C400-7 Antegrade Tibia 10¿ Bend, 10.0mm x 400mm, 7/10cm ST; 887517981318 BT10-10D360-5 Antegrade Femur Trochanter 10¿ Bend, 10.0mm x 360mm, 5/10cm ST; 887517981301 BT10-10D360-7 Antegrade Femur Trochanter 10¿ Bend, 10.0mm x 360mm, 7/10cm ST; 887517981295 BT10-10D380-5 Antegrade Femur Trochanter 10¿ Bend, 10.0mm x 380mm, 5/10cm ST; 887517981288 BT10-10D380-7 Antegrade Femur Trochanter 10¿ Bend, 10.0mm x 380mm, 7/10cm ST; 887517981271 BT10-10D400-5 Antegrade Femur Trochanter 10¿ Bend, 10.0mm x 400mm, 5/10cm ST; 887517981264 BT10-10D400-7 Antegrade Femur Trochanter 10¿ Bend, 10.0mm x 400mm, 7/10cm ST; 887517981257 BT10-10DT360-5 Antegrade Femur Trochanter 10¿ Bend, 10.0mm x 360mm, 5/10cm ST; 887517981240 BT10-10DT360-7 Antegrade Femur Trochanter 10¿ Bend, 10.0mm x 360mm, 7/10cm ST; 887517981233 BT10-10DT380-5 Antegrade Femur Trochanter 10¿ Bend, 10.0mm x 380mm, 5/10cm ST; 887517981226 BT10-10DT380-7 Antegrade Femur Trochanter 10¿ Bend, 10.0mm x 380mm, 7/10cm ST; 887517981219 BT10-10DT400-5 Antegrade Femur Trochanter 10¿ Bend, 10.0mm x 400mm, 5/10cm ST; 887517981202 BT10-10DT400-7 Antegrade Femur Trochanter 10¿ Bend, 10.0mm x 400mm, 7/10cm ST; 887517981196 BT10-10E360-5 Retrograde Femur Straight, 10.0mm x 360mm, 5/10cm ST; 887517981189 BT10-10E360-7 Retrograde Femur Straight, 10.0mm x 360mm, 7/10cm ST; 887517981172 BT10-10E380-5 Retrograde Femur Straight, 10.0mm x 380mm, 5/10cm ST; 887517981165 BT10-10E380-7 Retrograde Femur Straight, 10.0mm x 380mm, 7/10cm ST; 887517981158 BT10-10E400-5 Retrograde Femur Straight, 10.0mm x 400mm, 5/10cm ST; 887517981141 BT10-10E400-7 Retrograde Femur Straight, 10.0mm x 400mm, 7/10cm ST; 887517981134 BT10-10SA360-5 Retrograde Femur 5¿ Bend Three Holes, 10.0mm x 360mm, 5/10cm ST; 887517981127 BT10-10SA360-7 Retrograde Femur 5¿ Bend Three Holes, 10.0mm x 360mm, 7/10cm ST; 887517981110 BT10-10SA380-5 Retrograde Femur 5¿ Bend Three Holes, 10.0mm x 380mm, 5/10cm ST; 887517981103 BT10-10SA380-7 Retrograde Femur 5¿ Bend Three Holes, 10.0mm x 380mm, 7/10cm ST; 887517981097 BT10-10SA400-5 Retrograde Femur 5¿ Bend Three Holes, 10.0mm x 400mm, 5/10cm ST; 887517981080 BT10-10SA400-7 Retrograde Femur 5¿ Bend Three Holes, 10.0mm x 400mm, 7/10cm ST; 887517981073 BT10-10SB360-5 Recon Antegrade Femur Piriformis Straight, 10.0mm x 360mm, 5/10cm ST; 887517981066 BT10-10SB360-7 Recon Antegrade Femur Piriformis Straight, 10.0mm x 360mm, 7/10cm ST; 887517981059 BT10-10SB380-5 Recon Antegrade Femur Piriformis Straight, 10.0mm x 380mm, 5/10cm ST; 887517981042 BT10-10SB380-7 Recon Antegrade Femur Piriformis Straight, 10.0mm x 380mm, 7/10cm ST; 887517981035 BT10-10SB400-5 Recon Antegrade Femur Piriformis Straight, 10.0mm x 400mm, 5/10cm ST; 887517981028 BT10-10SB400-7 Recon Antegrade Femur Piriformis Straight, 10.0mm x 400mm, 7/10cm ST; 887517981011 BT10-10SD360-5 Recon Antegrade Femur Trochanter 10¿ Bend, 10.0mm x 360mm, 5/10cm ST; 88751… (truncated, 69135 characters total — see the official FDA record for the full value)
Recalling firm:
Nuvasive Specialized Orthopedics Inc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 12, 2021

NUVASIVE PRECICE Intramedullary Limb Lengthening (IMLL) and (Short) System End Cap for PRECICE Intramedullary Limb Lengthening System Implant; Packaged End Cap 8.5/10.7mm, +0mm; Packaged End Cap 8.5/10.7mm, +5mm; Packaged End Cap 8.5/10.7mm, +10mm; Packaged End Cap 8.5/10.7mm, +15mm; Packaged End Cap 8.5/10.7mm, +20mm; Packaged End Cap 12.5mm, +0mm; Packaged End Cap 12.5mm, +5mm; Packaged End Cap 12.5mm, +10mm; Packaged End Cap 12.5mm, +15mm; Packaged End Cap 12.5mm, +20mm; 3.5 mm Locking Screw, 20 mm Length; 3.5 mm Locking Screw 25 mm Length; 3.5 mm Locking Screw 30 mm Length; 3.5 mm Locking Screw 35 mm Length; 3.5 mm Locking Screw 40 mm Length; 3.5 mm Locking Screw 45 mm Length; 3.5 mm Locking Screw 50 mm Length; 3.5 mm Locking Screw 55 mm Length; 3.5 mm Locking Screw 60 mm Length; Locking Screw, 3.5x65mm; Locking Screw, 3.5x70mm; Locking Screw, 3.5x75mm; 4.0 mm Locking Screw 20 mm Length; 4.0 mm Locking Screw 25 mm Length; 4.0 mm Locking Screw 30 mm Length; 4.0 mm Locking Screw 35 mm Length; 4.0 mm Locking Screw 40 mm Length; 4.0 mm Locking Screw 45 mm Length; 4.0 mm Locking Screw 50 mm Length; 4.0 mm Locking Screw 55 mm Length; 4.0 mm Locking Screw 60 mm Length; 5.0 mm Locking Screw 20 mm Length; 5.0 mm Locking Screw 25 mm Length; 5.0 mm Locking Screw 30 mm Length; 5.0 mm Locking Screw 35 mm Length; 5.0 mm Locking Screw 40 mm Length; 5.0 mm Locking Screw 45 mm Length; 5.0 mm Locking Screw 50 mm Length; 5.0 mm Locking Screw 55 mm Length; 5.0 mm Locking Screw 60 mm Length; 5.0 mm Locking Screw 65 mm Length; 5.0 mm Locking Screw 70 mm Length; 5.0 mm Locking Screw 75 mm Length; 4.0 mm Locking Screw 20 mm Length; 4.0 mm Locking Screw 25 mm Length; 4.0 mm Locking Screw 30 mm Length; 4.0 mm Locking Screw 35 mm Length; 4.0 mm Locking Screw 40 mm Length; 4.0 mm Locking Screw 45 mm Length; 4.0 mm Locking Screw 50 mm Length; 4.0 mm Locking Screw 55 mm Length; 4.0 mm Locking Screw 60 mm Length; 4.0 mm X 65 mm Locking Screw, Peg; 4.0 mm X 70 mm Locking Screw, Peg; 4.0 mm X 75 mm Locking Screw, Peg; 4.0 mm X 80 mm Locking Screw, Peg; 4.0 mm X 85 mm Locking Screw, Peg; 4.0 mm X 90 mm Locking Screw, Peg; 4.0 mm X 95 mm Locking Screw, Peg; 4.0 mm X 100 mm Locking Screw, Peg; 5.0 mm Locking Screw 20 mm Length; 5.0 mm Locking Screw 25 mm Length; 5.0 mm Locking Screw 30 mm Length; 5.0 mm Locking Screw 35 mm Length; 5.0 mm Locking Screw 40 mm Length; 5.0 mm Locking Screw 45 mm Length; 5.0 mm Locking Screw 50 mm Length; 5.0 mm Locking Screw 55 mm Length; 5.0 mm Locking Screw 60 mm Length; 5.0 mm Locking Screw 65 mm Length; 5.0 mm Locking Screw 70 mm Length; 5.0 mm Locking Screw 75 mm Length; 5.0 mm X 80 mm Locking Screw, Peg; 5.0 mm X 85 mm Locking Screw, Peg; 5.0 mm X 90 mm Locking Screw, Peg; 5.0 mm X 95 mm Locking Screw, Peg; 5.0 mm X 100 mm Locking Screw, Peg; Orthopedic intramedullary limb lengthening rod, retrograde femur 10 degree, 10.7 mm diameter, 170 mm length; Orthopedic intramedullary limb lengthening rod, antegrade tibia, 10.7 mm diameter, 160 mm length; Orthopedic intramedullary limb lengthening rod, antegrade femur trochanteric, 10.7 mm diameter, 170 mm length; Orthopedic intramedullary limb lengthening rod, universal femur, 10.7 mm diameter, 170 mm length; Orthopedic intramedullary limb lengthening rod, retrograde femur, 10 degree, 10.7 mm diameter, 215 mm length; Orthopedic intramedullary limb lengthening rod, retrograde femur, 10 degree, 10.7 mm diameter, 230 mm length; Orthopedic intramedullary limb lengthening rod, antegrade femur (piriformis), 10.7 mm diameter, 215 mm length; Orthopedic intramedullary limb lengthening rod, antegrade femur (piriformis), 10.7 mm diameter, 230 mm length; Orthopedic intramedullary limb lengthening rod, antegrade tibia, 10.7 mm diameter, 195 mm length; Orthopedic intramedullary limb lengthening rod, antegrade tibia, 10.7 mm diameter, 215 mm length; Orthopedic intramedullary limb lengthening

Due to not having the full complement of biological assessments for all potential patients and as a result the devices are not indicated for use in individuals under the age of 18 years old.

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FDA has not published a risk classification for this recall yet.

Recall #:
87353
Lot/product code:
All Lots manufactured between April 2015 to February 2021.  PRECICE Intramedullary Limb Lengthening (IMLL) Product Codes:  End caps: CPA1-000; CPA2-000; CPA2-005; CPA2-010; CPA2-015; CPA2-020; CPA3-000; CPA3-005; CPA3-010; CPA3-015; CPA3-020;  Locking screws:  LSB3-020; LSB3-025; LSB3-030; LSB3-035; LSB3-040; LSB3-045; LSB3-050; LSB3-055; LSB3-060; LSB3-065; LSB3-070; LSB3-075; LSB4-020; LSB4-025; LSB4-030; LSB4-035; LSB4-040; LSB4-045; LSB4-050; LSB4-055; LSB4-060; LSB5-020; LSB5-025; LSB5-030; LSB5-035; LSB5-040; LSB5-045; LSB5-050; LSB5-055; LSB5-060; LSB5-065; LSB5-070; LSB5-075; LSC4-020; LSC4-025; LSC4-030; LSC4-035; LSC4-040; LSC4-045; LSC4-050; LSC4-055; LSC4-060; LSC4-065; LSC4-070; LSC4-075; LSC4-080; LSC4-085; LSC4-090; LSC4-095; LSC4-100; LSC5-020; LSC5-025; LSC5-030; LSC5-035; LSC5-040; LSC5-045; LSC5-050; LSC5-055; LSC5-060; LSC5-065; LSC5-070; LSC5-075; LSC5-080; LSC5-085; LSC5-090; LSC5-095; LSC5-100;   Limb lengthening intramedullary rods 10.7 mm diameter:  P10.7-30H170; P10.7-30J160; P10.7-30K170; P10.7-30U170; P10.7-50A215; P10.7-50A230; P10.7-50B215; P10.7-50B230; P10.7-50C195; P10.7-50C215; P10.7-50C230; P10.7-50D215; P10.7-50D230; P10.7-50E215; P10.7-50E230; P10.7-50H190; P10.7-50J180; P10.7-50K190; P10.7-50M175; P10.7-50N160; P10.7-50P175; P10.7-50Q155; P10.7-50U190; P10.7-50V215; P10.7-50V230; P10.7-50X215; P10.7-50X230; P10.7-80A245; P10.7-80A275; P10.7-80A305; P10.7-80A335; P10.7-80A365; P10.7-80B245; P10.7-80B275; P10.7-80B305; P10.7-80B335; P10.7-80B365; P10.7-80C245; P10.7-80C275; P10.7-80C305; P10.7-80C335; P10.7-80C365; P10.7-80D245; P10.7-80D275; P10.7-80D305; P10.7-80D335; P10.7-80D365; P10.7-80E245; P10.7-80E275; P10.7-80E305; P10.7-80E335; P10.7-80E365; P10.7-80V245; P10.7-80V275; P10.7-80V305; P10.7-80V335; P10.7-80V365; P10.7-80X245; P10.7-80X275; P10.7-80X305; P10.7-80X335; P10.7-80X365;   Limb lengthening intramedullary rods 12.5 mm diameter:  P12.5-30H170; P12.5-30J160; P12.5-30K170; P12.5-30U170; P12.5-50A215; P12.5-50A230; P12.5-50B215; P12.5-50B230; P12.5-50C195; P12.5-50C215; P12.5-50C230; P12.5-50D215; P12.5-50D230; P12.5-50E215; P12.5-50E230; P12.5-50H190; P12.5-50J180; P12.5-50K190; P12.5-50U190; P12.5-50V215; P12.5-50V230; P12.5-50X215; P12.5-50X230; P12.5-80A245; P12.5-80A275; P12.5-80A305; P12.5-80A335; P12.5-80A365; P12.5-80B245; P12.5-80B275; P12.5-80B305; P12.5-80B335; P12.5-80B365; P12.5-80C245; P12.5-80C275; P12.5-80C305; P12.5-80C335; P12.5-80C365; P12.5-80D245; P12.5-80D275; P12.5-80D305; P12.5-80D335; P12.5-80D365; P12.5-80E245; P12.5-80E275; P12.5-80E305; P12.5-80E335; P12.5-80E365; P12.5-80V245; P12.5-80V275; P12.5-80V305; P12.5-80V335; P12.5-80V365; P12.5-80X245; P12.5-80X275; P12.5-80X305; P12.5-80X335; P12.5-80X365;   Limb lengthening intramedullary rods 8.5 mm diameter:  P8.5-30H170; P8.5-30J160; P8.5-30K170; P8.5-30U170; P8.5-50A215; P8.5-50A230; P8.5-50B215; P8.5-50B230; P8.5-50C195; P8.5-50C215; P8.5-50C230; P8.5-50D215; P8.5-50D230; P8.5-50E215; P8.5-50E230; P8.5-50H190; P8.5-50J180; P8.5-50K190; P8.5-50M165; P8.5-50N150 P8.5-50P165; P8.5-50Q155; P8.5-50U190; P8.5-50V215; P8.5-50V230; P8.5-50X215; P8.5-50X230; P8.5-80A245; P8.5-80A275; P8.5-80A305; P8.5-80A335; P8.5-80A365; P8.5-80B245; P8.5-80B275; P8.5-80B305; P8.5-80B335; P8.5-80B365; P8.5-80C245; P8.5-80C275; P8.5-80C305; P8.5-80C335; P8.5-80C365; P8.5-80D245; P8.5-80D275; P8.5-80D305; P8.5-80D335; P8.5-80D365; P8.5-80E245; P8.5-80E275; P8.5-80E305; P8.5-80E335; P8.5-80E365; P8.5-80V245; P8.5-80V275; P8.5-80V305; P8.5-80V335; P8.5-80V365; P8.5-80X245; P8.5-80X275; P8.5-80X305; P8.5-80X335; P8.5-80X365;    Limb lengthening intramedullary rods 10.5 mm diameter:  PR10.5-50A215; PR10.5-50A230; PR10.5-50B215; PR10.5-50B230; PR10.5-50C195; PR10.5-50C215; PR10.5-50C230; PR10.5-50D215; PR10.5-50D230; PR10.5-50E215; PR10.5-50E230; PR10.5-80A245; PR10.5-80A275; PR10.5-80A305; PR10.5-80A335; PR10.5-80A365; PR10.5-80B245; PR10.5-80B275; PR10.5-80B305; PR10.5-80B335; PR10.5-80B365; PR10.5-80C245; PR10.5-80C275; PR10.5-80C305; PR10.5-80C335; PR10.5-80C365; PR10.5-80D245; PR10.5-80D275; PR10.5-80D305; PR10.5-80D335; PR10.5-80D365; PR10.5-80E245; PR10.5-80E275; PR10.5-80E305; PR10.5-80E335; PR10.5-80E365;    Limb lengthening intramedullary rods 11.5 mm diameter:  PR11.5-50A215; PR11.5-50A230; PR11.5-50B215; PR11.5-50B230; PR11.5-50C195; PR11.5-50C215; PR11.5-50C230; PR11.5-50D215; PR11.5-50D230; PR11.5-50E215; PR11.5-50E230; PR11.5-80A245; PR11.5-80A275; PR11.5-80A305; PR11.5-80A335; PR11.5-80A365; PR11.5-80B245; PR11.5-80B275; PR11.5-80B305; PR11.5-80B335; PR11.5-80B365; PR11.5-80C245; PR11.5-80C275; PR11.5-80C305; PR11.5-80C335; PR11.5-80C365; PR11.5-80D245; PR11.5-80D275; PR11.5-80D305; PR11.5-80D335; PR11.5-80D365; PR11.5-80E245; PR11.5-80E275; PR11.5-80E305; PR11.5-80E335; PR11.5-80E365;   Limb lengthening intramedullary rods 12.5 mm diameter:  PR12.5-50A215; PR12.5-50A230; PR12.5-50B215; PR12.5-50B230; PR12.5-50C195; PR12.5-50C215; PR12.5-50C230; PR12.5-50D215; PR12.5-50D230; PR1… (truncated, 19741 characters total — see the official FDA record for the full value)
Recalling firm:
Nuvasive Specialized Orthopedics Inc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 18, 2021

RUSCH POLARIS" Laryngoscope - Product Usage: intended to allow direct visualization of the laryngeal structure and is used during tracheal intubation.

Teleflex is voluntarily recalling the products referenced above due to customers reporting that the laryngoscope handles develop cracks and/or break at the hinge.

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FDA has not published a risk classification for this recall yet.

Recall #:
87370
Lot/product code:
Model 44401 (GTIN: Each: 14026704662552 Box: 24026704662559 Case: 34026704662556; lots 197, 19A, 19F, 19J, 19P, 19W, 205, 207, 20C, 20H, 20T); Model 44402 (GTIN: Each: 14026704662569 Box: 24026704662566 Case: 34026704662563; lots 197, 19A, 19F, 19J, 19P, 19W, 205, 207, 20C, 20H, 20M, 20T);  Model 44403 (GTIN: Each: 14026704662576 Box: 24026704662573 Case: 34026704662570; lots 197, 19A, 19F, 19J, 207, 20C, 20H, 20M, 20T).
Recalling firm:
TELEFLEX MEDICAL INC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 22, 2021

Mindray BeneVision Distributed Monitoring System( DMS) 1. p/n 115-051209-00 2. p/n 115-034414-00 and 115-034413-00 when used with the following software versions: 03.04.00 04.01.00 04.03.00 04.04.00 04.04.01

BeneVision DMS may intermittently freeze and require a manual reboot after which normal operation resumes. If a freeze occur, patients monitored on a telemetry transmitter will no longer communicate data to the BeneVision DMS

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FDA has not published a risk classification for this recall yet.

Recall #:
87380
Lot/product code:
Serial Numbers: EHT92003259 EHL5A000498 EHL61000561 EHL67000842 EHL67000843 EHM67000809 EHT04004409 EHT04004412 EHT0A004549 EHT94003329 EHT94003338 EHT94003342 EHT96003496 EHT9C003918 EHT9C003920 EHL64000627 EHL64000629 EHL64000622 EHL65000697 EHL6B001060 EHL6B001063 EHL6B001069 EHM6C001164 EHL74001282 EHM86002739 EHL5B000545 EHL78001536 EHT07004512 EHT8A002987 EHT02004001 EHT87002783 EHT87002784 EHL5A000463 EHT04004422 EHT92003257 EHL65000729 EHM69000971 EHT89002847 EHT89002850 EHT89002860 EHT87002781 EHL75001349 EHM74001293 EHM75001343 EHL74001301 EHL78001509 EHM69000970 EHT0A004556 EHT8A002980 EHL5A000532 EHM67000801 EHT91003190 EHT99003784 EHL73001200 EHL73001205 EHL73001207 EHT94003326 EHL79001585 EHM7B001731 EHL5A000526 EHL5B000543 EHL65000717 EHL65000721 EHT96003499 EHT88002799 EHT94003339 EHT96003503 EHT9C003922 EHL83002385 EHL81002225 EHL83002304 EHL83002310 EHL74001311 EHL83002387 EHL67000845 EHL73001197 EHL73001198 EHL73001199 EHM67000777 EHM68000887 EHT91003180 EHT91003181 EHT96003500 EHL84002434 EHT06004482 EHL68000900 EHT89002851 EHT89002853 EHT89002855 EHT89002861 EHT04004425 EHT04004410 EHL59000404 EHT92003244 EHL59000382 EHL5B000546 EHL5B000547 EHL65000704 EHL69000931 EHL72001179 EHL77001466 EHT8C003065 EHT8C003066 EHT8C003068 EHT07004496 EHT07004505 EHT88002796 EHL77001469 EHT91003182 EHT91003183 EHT96003540 EHT92003245 EHT92003250 EHT92003251 EHL76001382 EHL79001605 EHL6C001118 EHL65000727 EHL74001312 EHM68000895 EHM68000910 EHT97003624 EHT99003779 EHT99003780 EHL83002405 EHT88002786 EHT94003337 EHL76001383 EHL76001386 EHL76001390 EHL76001392 EHL77001481 EHL77001482 EHL77001483 EHL77001484 EHM74001273 EHM74001297 EHM76001377 EHM76001378 EHL5A000490 EHL5A000496 EHT06004490 EHL67000827 EHT8C003052 EHL73001225 EHL73001231 EHM6A001051 EHM6A001053 EHM6C001096 EHM77001488 EHL84002433 EHL81002219 EHL83002297 EHL83002298 EHL73001209 EHM78001517 EHM68000886 EHL68000902 EHL62000584 EHL61000566 EHL7A001641 EHM7A001666 EHL5A000458 EHL5A000534 EHL81002222 EHL76001387 EHL7A001690 EHL65000723 EHT85002591 EHL74001299 EHT94003336 EHL64000620 EHL64000621 EHL64000623 EHL64000625 EHL64000626 EHL64000638 EHL76001418 EHL76001421 EHL76001423 EHM7B001733 EHL81002227 EHT86002720 EHT86002721 EHT86002723 EHT86002728 EHT88002788 EHT0A004540 EHL79001546 EHL79001602 EHM78001516 EHM7A001686 EHL81002230 EHT96003542 EHL74001314 EHT04004421 EHT04004462 EHT04004469 EHT04004416 EHT04004417 EHL7B001746 EHL7C001758 EHL65000694 EHT0A004541 EHL67000825 EHL67000826 EHL67000828 EHL67000833 EHL67000834 EHL68000903 EHL68000904 EHL68000905 EHL68000906 EHL68000908 EHT96003541 EHT99003785 EHL72001189 EHT04004419 EHL63000595 EHL67000846 EHL6A001014 EHL6C001110 EHM67000808 EHM68000890 EHM68000891 EHT0A004550 EHL6A001039 EHL73001227 EHL73001229 EHL73001230 EHL73001232 EHM69000924 EHM69000926 EHM6A001052 EHM6A001054 EHM6C001093 EHM6C001094 EHL79001545 EHL79001547 EHM77001491 EHM7C001770 EHL7A001650 EHL6A001035 EHM68000894 EHL65000699 EHL7B001747 EHL83002407 EHL84002435 EHM81002042 EHM86002738 EHT04004418 EHT87002763 EHT88002806 EHL83002390 EHL83002392 EHL5A000486 EHL5A000516 EHL62000575 EHL62000582 EHL63000596 EHL63000598 EHL63000600 EHL63000601 EHL63000602 EHL67000832 EHM68000888 EHM68000914 EHL75001348 EHL81002226 EHM75001330 EHT06004488 EHM74001298 EHL79001544 EHT92003242 EHT96003501 EHT9C003919 EHT8C003062 EHL5A000478 EHL5A000484 EHT04004413 EHT8A002979 EHT8A002981 EHT89002849 EHL7C001762 EHL7C001917 EHT8C003060 EHT0A004559 EHT85002581 EHT85002583 EHT95003468 EHL65000751 EHL69000929 EHL6B001071 EHL6B001072 EHM68000916 EHT92003249 EHT94003335 EHL77001467 EHL5A000520 EHL5A000525 EHM74001272 EHM74001318 EHL6A001034 EHL83002299 EHT0A004560 EHL7C001761 EHL84002439 EHT86002732 EHL7A001649 EHL7A001652 EHM7B001736 EHM7B001740 EHL77001465 EHL77001473 EHM95003470 EHM96003571 EHL83002389 EHL75001358 EHM74001292 EHL5A000497 EHL5A000514 EHL62000570 EHL5A000528 EHL75001360 EHM75001344 EHT03004115 EHT8C003049 EHT06004487 EHL76001417 EHT99003823 EHL59000403 EHL59000406 EHL59000408 EHL7A001658 EHM81002039 EHL5B000542 EHL6A001001 EHT92003248 EHL75001357 EHL78001535 EHL78001537 EHL78001538 EHT04004467 EHT8C003050 EHT96003533 EHT96003543 EHL7A001700 EHT99003824 EHL67000824 EHM68000912 EHT95003469 EHL73001208 EHM75001338 EHT88002797 EHT8A002986 EHL83002309 EHT94003332 EHL7A001692 EHT88002812 EHT96003532 EHT88002814 EHT88002809 EHT99003783 EHL74001321 EHL74001326 EHM74001270 EHT9C003921 EHL7A001696 EHT92003247 EHL74001309 EHL75001350 EHL5A000523 EHL59000366 EHL59000374 EHL59000383 EHL5A000521 EHM74001294 EHL5A000466 EHL74001302 EHL74001306 EHL75001356 EHM74001289 EHL79001604 EHM7A001687 EHT88002791 EHL7A001699 EHL7C001921 EHL83002403 EHM6A001043 EHL67000822 EHL67000831 EHM67000810 EHM69000952 EHM69000954 EHM69000955 EHM69000956 EHT88002787 EHL5A000480 EHT9C003926 EHT9C003927 EHL78001512 EHM78001515 EHL63000617 EHT06004483 EHL59000409 EHL7C001760 EHM85002683 EHL7C001759 EHL7C001904 EHM76001372 EHT03004116 EHT03004117 EHL61000562 EHL78001510 EHM75001332 EHM7… (truncated, 13660 characters total — see the official FDA record for the full value)
Recalling firm:
Mindray DS USA, Inc. dba Mindray North America
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 22, 2021

EPIX Therapeutics DiamondTemp Bidrectional Small Curve Ablation Catheter, 7.5 French Size(2.48 mm), Connector Type: ODU 19 PIN, REF:CEDTB300S, SterileEO, UDI: 00812499030358

It has been identified that the catheter size on the packaging labeling does not correspond to the widest part of the catheter. In addition the IFU contains the incorrect diameter of the catheter. This could result in blood stagnation, clots or air emboli.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
87412
Lot/product code:
All Lots
Recalling firm:
EPIX THERAPEUTICS, INC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 22, 2021

EPIX Therapeutics DiamondTemp Unidirectional Small Curve Ablation Catheter, 7.5 French Size(2.48 mm), Connector Type: ODU 19 PIN, REF CEDT100S, SterileEO, UDI 00812499030198

It has been identified that the catheter size on the packaging labeling does not correspond to the widest part of the catheter. In addition the IFU contains the incorrect diameter of the catheter. This could result in blood stagnation, clots or air emboli.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
87412
Lot/product code:
All Lots
Recalling firm:
EPIX THERAPEUTICS, INC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 22, 2021

EPIX Therapeutics DiamondTemp Bidrectional Large Curve Ablation Catheter, 7.5 French Size(2.48 mm), Connector Type: ODU 19 PIN, REF:CEDTB400L, SterileEO, UDI: 00812499030303

It has been identified that the catheter size on the packaging labeling does not correspond to the widest part of the catheter. In addition the IFU contains the incorrect diameter of the catheter. This could result in blood stagnation, clots or air emboli.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
87412
Lot/product code:
All Lots
Recalling firm:
EPIX THERAPEUTICS, INC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 22, 2021

EPIX Therapeutics DiamondTemp Unidirectional Large Curve Ablation Catheter, 7.5 French Size(2.48 mm), Connector Type: ODU 19 PIN, REF: CEDT200L, Sterile EO, UDI: 00812499030259

It has been identified that the catheter size on the packaging labeling does not correspond to the widest part of the catheter. In addition the IFU contains the incorrect diameter of the catheter. This could result in blood stagnation, clots or air emboli.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
87412
Lot/product code:
All Lots
Recalling firm:
EPIX THERAPEUTICS, INC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 22, 2021

EPIX Therapeutics DiamondTemp Unidirectional Ablation Catheter, Small Curve, 7.5 French Size(2.48 mm), Connector Type: ODU 19 PIN, REF:DT100S,SterileEO, Rx Only, UDI: 00812499030006

It has been identified that the catheter size on the packaging labeling does not correspond to the widest part of the catheter. In addition the IFU contains the incorrect diameter of the catheter. This could result in blood stagnation, clots or air emboli.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
87412
Lot/product code:
All Lots
Recalling firm:
EPIX THERAPEUTICS, INC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 22, 2021

EPIX Therapeutics DiamondTemp Unidirectional Ablation Catheter, Large Curve, 7.5 French Size(2.48 mm), Connector Type: ODU 19 PIN, REF:DT200L, SterileEO, Rx Only, UDI: 00812499030013

It has been identified that the catheter size on the packaging labeling does not correspond to the widest part of the catheter. In addition the IFU contains the incorrect diameter of the catheter. This could result in blood stagnation, clots or air emboli.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
87412
Lot/product code:
All Lots
Recalling firm:
EPIX THERAPEUTICS, INC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 26, 2021

Medtronic REF: MMT-7020C5 Guardian Sensor (3) for the following packaging: GS3 5PK 1L AUS/ GTIN: 20763000252056 GS3 5PK 1L AUS/ GTIN: 20763000414362 Product Usage: intended for use with Medtronic Diabetes (Medtronic) glucose sensing systems to continuously monitor glucose levels in persons with diabetes. Product Usage: intended for use with Medtronic Diabetes (Medtronic) glucose sensing systems to continuously monitor glucose levels in persons with diabetes. *Product not distributed within US.

Use of the continuous glucose monitoring system while actively taking hydroxyurea, an anti-neoplastic drug could result in inaccurate elevated sensor glucose readings.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
87476
Lot/product code:
All Lot numbers within active shelf life
Recalling firm:
Medtronic Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 26, 2021

Medtronic REF: MMT-7020C3 Guardian Sensor (3) for the following packaging: GS3 5PK OUS3/ GTIN: 20643169704118 GS3 5PK 9L OUS3/ GTIN: 20763000243368 GS3 5PK 9L OUS3/ GTIN: 20763000318882 Product Usage: intended for use with Medtronic Diabetes (Medtronic) glucose sensing systems to continuously monitor glucose levels in persons with diabetes. *Product not distributed within US.

Use of the continuous glucose monitoring system while actively taking hydroxyurea, an anti-neoplastic drug could result in inaccurate elevated sensor glucose readings.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
87476
Lot/product code:
All Lot numbers within active shelf life
Recalling firm:
Medtronic Inc.
View official FDA record (opens in a new tab)