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Recalls affecting Maryland

Data last updated: September 11, 2026 at 1:08 PM UTC

16,861 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

View FDA’s announcement (opens in a new tab)
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 July 20, 2021

HARMONIC HD 1000i Shears (20cm Shaft Length)-indicated for soft tissue incisions when bleeding control and minimal thermal injury are desired. Product Code: HARHD20

An internal component may be cracked and become lodged behind the energy button potentially resulting in continuous activation of the device, may result in burns

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

Recall #:
88434
Lot/product code:
Lot Codes: U95126 U9571N U9526Z U95A80 U9543P U95T0X U9550G GTIN: 10705036015048
Recalling firm:
Ethicon Endo-Surgery Inc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled July 20, 2021

CritiCool, thermoregulation device

Premature pump failure may lead to the device displaying a HALT 4 error, from which the device cannot recover even after device reboot. The issue may potentially lead to delayed treatment and a failure to deliver the prescribed thermoregulation therapy. To date, the firm has received one report of death potentially related to this issue.

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

Recall #:
90939
Lot/product code:
UDI-DI: 07290107581110 Serial Numbers: 9978580900011 99110698100043 99110698100044 9963715800012 9982077400003 9971040500004 9982294100006 9964294500006 9963715800008 9964294500007 9978580900008 9978580900009 9999186600019 99110008800035 99110008800036 99109321700020 99109321700026 99110992900020 99100663300011 99100663300014 99101637500005 99110698100048 9966227400007 9966227400012 9989990200008 9995915300007 9995915300014 9966227400008 9966227400011 9969231000003 9969231000004 9969231000005 9969570100004 9969570100014 9969570100018 99108208900030 99109321700010 9989990200012 99110992900011 9974072400005 99102316800013 9974085100011 9995355700003 99108208900023 99108208900025 996622740007 9969570100016 99104180900007 99107291500013 99107291500016 9983874900002 99108208900022 99109321700004 9978471200014 99100663300013 99100663300023 9995355500001 9995355500001 9995355500003 9995355500003 9996480200001 99104183000019 99104183000021 99110698100028 99110698100029 9982315400005 9982315400007 99110992900003 99110992900004 99110992900005 9964294500014 99102316800010 9999186600018 9999186600020 99100663300024 9974085100004 9989990200007 9995355500007 9974085100001 9974085100005 9974085100007 9974085100008 9974085100017 9974085100018 9974085100022 9974085100023 9974085100026 9975437700001 9969570200002 9969570100020 9976535500007 9976535500002 9986341600006 9986341600007 9986341600008 9975437700020 9981876000006 9981876000008 9982077400005 9982077400007 9982077400001 9995355600002 99110992900012 99110992900013 9995355500006 9986341600011 9988633600001 9988633600016 9973538600014 9978580900010 99104728800017 9964294500017 9976535500004 99100663300026 9964294500004 9969414800006 99109321700019 99108045000012 99108045000026 99108045000028 9973538500009 9974072400008 9982077400004 9982294100004 9982294100005 9999186600010 9999186600008 9971554000008 9971554000010 9982294100009 9963715800014 99110992900017 9969570200011 9971040400008 9971473300015 9982294100013 9975437700015 9976535500003 99110698100019 99110698100020 9963715800016 9964995000015 9975437700003 99108208900012 99100663300003 99104728800016 9966227400013 99104183000018 99104183000027 99110698100049 99110992900008 99110992900019 99103245000021 9969414800020 9964294500019 9986341600005 9995355500002 9999186600015 9991825100005 9991825100023 9992010100005 9992015300005 9992015300008 9996480200004 9995915300002 9995915300009 9966227400005 9966227400004 9969414800009 9969414800016 9969570100008 9969570100009 9969570100010 9969570100013 9971040400010 9971040500006 9971040500015 9971473300001 9971473300002 9971473300003 9971473300004 9971473300010 9971554000007 9973538500001 9973538500004 9973538500005 9973538500010 99110698100046 99110698100047 99110698100050 9969414800014 9973538600006 9976535500010 99110698100037 99108208900021 99101637500007 99102316800001 99101637500010 99102316800011 99104728800008 99104183000035 99104728000020 99104728800022 99104728800023 99104728800024 99104728800025 99104728800026 99110008800007 99110008800008 99110008800004 99110008800027 99108045000008 99109321700049 99109321700034 99110008800001 99110008800003 99110008800006 99109321700050 99110008800005 99109321700047 99109321700028 99109321700042 99109321700041 99109321700043 99109321700044 99110698100042 9974072400011 9974085100019 9995355700005 9995355700010 9995355700001 9995915300004 9995915300006 9995915300010 9995915300012 9995915300013 9996480200010 9996480200011 9996480200013 9996791600008 9996791600009 9996791600010 9999186600001 99104183000001 99104183000002 99104183000003 99104183000004 99104728800013 99104728800019 99104728800031 99107291500001 99107291500004 99110008800002 99110008800019 99110008800011 99110008800012 99110008800013 99110008800028 99110008800009 99110008800010 99110008800026 99110008800030 99109321700012 9971040500010 999535550001 999535550003 999535550004 999535550005 9.91016E+13 9.91042E+13 9.91047E+13 9.91082E+13 9.91082E+13 99110698100045 99110992900018 99110992900015 9954452900016 9961427900008 9969231000001 9969414800004 9969414800005 9969414800001 9977251300007 9977251300008 9977251300006 9977251300005 9977251300004 9977251300003 9964294500002 9966227400014 9969231000006 9969570200010 9969570200014 9979841600011 9978471200001 9978471200022 9981876000007 9988633600009 9989990200009 9992015300006 99102316800021 99104180900001 99110698100021 9993901400005 9979841600006 9979841600017 9970259900001 9969570200008 9971040400002 9971040400003 9973538500002 9973538500003 9973538500007 9979841600008 9978471200029 9981876000002 9981876000003 9981876000004 9982077400002 9983349200009 9983349200012 9983349300008 9983349300011 9983349300012 9983349300014 9986341500004 9983874900011 9986341500003 9986341500001 9996791600002 9996791600005 99100663300021 99100663300010 99100663300022 99100663300025 99101637500002 9910324500009 9910324500007 9910324500010 9910324500006 9910324500012 99107291500019 99107291500014 99107291500015 99107291500008 99108045000009 9910820… (truncated, 13802 characters total — see the official FDA record for the full value)
Recalling firm:
Belmont Instrument Corporation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled July 20, 2021

Braun ThermoScan PRO 6000 Ear Thermometer-indicated for the intermittent measurement of human body temperature for patients having ages ranging from normal weight (full term) newborn to geriatric adults in a professional use environment. Model: 6000

If the device is exposed to fluid ingress and is used before the cleaning fluid has completely dried, there is a risk of the device overheating potentially causing a burn to the user or the ear canal of the patient

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

Recall #:
88481
Lot/product code:
All Devices in distribution. UDI: 00732094309027 DDDYYKXXXXX DDD = 3 DIGIT JULIAN DAY (EXAMPLE - 234). YY = LAST 2 DIGITS OF JULIAN YEAR (EXAMPLE - 13) K = KEYTRONIC XXXXX = 5 DIGIT BASE 10 SERIALIZED NUMBER.
Recalling firm:
Welch Allyn Inc
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled July 20, 2021

Miss Slim, capsules, packaged in 10-count and 30-count box, Distributed by : His Enterprise Made in USA UPC 742137605030

Marketed without ANDA/NDA approval

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A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0770-2021
Lot/product code:
all lots
Recalling firm:
HIS ENTERPRISE INC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled July 21, 2021

CS9600isanextraoralsystemintendedtoproducetwo-dimensionalandthree-dimensionaldigitalX-rayimagesofthedento-maxilofacial,ENT(Ear,NoseandThroat),cervicalspineandwristregionsatthedirectionofhealthcareprofessionalsasdiagnosticsupportforpediatricandadultpatients.

Device failed to function as intended and/or failed to conform to their design specifications.

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

Recall #:
92206
Lot/product code:
CS 9600
Recalling firm:
Trophy SAS
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled July 22, 2021

EPIQ Ultrasound Systems, Model: EPIQ Elite, EPIQ 5G, EPIQ 5C, EPIQ 5W, EPIQ 7G, EPIQ 7C, EPIQ 7W, EPIQ CVx, EPIQ CVxi

Ultrasound system control panel arm swivel lock could fail, which could cause the control panel and monitor to swivel freely while a user is positioning the monitor, or transporting/moving the system, which could lead to patient or user musculoskeletal injury.

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

Recall #:
88313
Lot/product code:
Manufactured Between 2020-02-27 to 2021-05-25
Recalling firm:
Philips Ultrasound Inc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled July 23, 2021

TheraSphere Administration Set, REF OTT-SPE-FP-001 (990264.SPE)

Potential for leaks and loosening at the patient catheter connection

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▸Full report

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

Recall #:
88369
Lot/product code:
GTIN 05060116920635, Lot Numbers: 61673698, 61673699, 61673700, 61673702, 61694124, 61705932, 61706656, 61705933, 61732176
Recalling firm:
Boston Scientific Corporation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled July 23, 2021

TheraSphere Administration Set, REF OTT-SPE-FP-226 (990226.SPE)

Potential for leaks and loosening at the patient catheter connection

ALL 50 STATES
▸Full report

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

Recall #:
88369
Lot/product code:
GTIN 05060116920253, Lot Numbers: 001E, 002E, 004E, 005E, 006E, 007E, 114E, 690E, 692E
Recalling firm:
Boston Scientific Corporation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled July 26, 2021

Trilogy EV300, Product numbers CA2200X12B, DS2200X11B, FX2200X15B, IN2200X15B

Two software issues have been identified related to pressure increase in the device: The first issue is described as "Infant/Pediatric EFS Calibration Pressure Increase" and the second issue is described as "Pressure Drift (Continuous Usage).

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▸Full report

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

Recall #:
88333
Lot/product code:
Software version numbers 1.02.01.00, 1.03.05.00, 1.03.07.00, 1.04.02.00, 1.04.06, 1.05.01, and 1.06.02
Recalling firm:
Philips Respironics, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled July 26, 2021

Trilogy Evo Universal, Product number DS2000X11B

Two software issues have been identified related to pressure increase in the device: The first issue is described as "Infant/Pediatric EFS Calibration Pressure Increase" and the second issue is described as "Pressure Drift (Continuous Usage).

ALL 50 STATES
▸Full report

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

Recall #:
88333
Lot/product code:
Software version numbers 1.02.01.00, 1.03.05.00, 1.03.07.00, 1.04.02.00, 1.04.06, 1.05.01, and 1.06.02
Recalling firm:
Philips Respironics, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled July 26, 2021

Trilogy Evo O2, Product numbers DE2100X13B, DS2100X11B, EE2100X15B, ES2100X15B, EU2100X15B, FR2100X14B, FX2100X15B, IA2100X15B, IN2100X15B, IN2100X19, IT2100X21B, JP2100X16B, LA2100X15B, ND2100X15B, RDE2100X13B, SP2100X26B

Two software issues have been identified related to pressure increase in the device: The first issue is described as "Infant/Pediatric EFS Calibration Pressure Increase" and the second issue is described as "Pressure Drift (Continuous Usage).

ALL 50 STATES
▸Full report

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

Recall #:
88333
Lot/product code:
Software version numbers 1.02.01.00, 1.03.05.00, 1.03.07.00, 1.04.02.00, 1.04.06, 1.05.01, and 1.06.02
Recalling firm:
Philips Respironics, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled July 26, 2021

Trilogy Evo, Product numbers BL2110X15B, CA2110X12B, DE2110X13B, DS2110X11B, EE2110X15B, ES2110X15B, EU2110X15B, EU2110X19, FR2110X14B, GB2110X15B, IA2110X15B, IN2110X15B, IN2110X19, IT2110X21B, KR2110X15B, LA2110X15B, LD2110X23B, ND2110X15B, RDE2110X13B, UDS2110X11B

Two software issues have been identified related to pressure increase in the device: The first issue is described as "Infant/Pediatric EFS Calibration Pressure Increase" and the second issue is described as "Pressure Drift (Continuous Usage).

ALL 50 STATES
▸Full report

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

Recall #:
88333
Lot/product code:
Software version numbers 1.02.01.00, 1.03.05.00, 1.03.07.00, 1.04.02.00, 1.04.06, 1.05.01, and 1.06.02
Recalling firm:
Philips Respironics, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled July 26, 2021

Alinity ci-series System Control Module clinical chemistry and immunoassay analyzer for in vitro diagnostic use. Model number LN 03R70-01

Due to potential performance issues with software version 3.2.3 and earlier. Performance issues are: 1) There is the potential for onboard reagents past their lot expiration date or onboard stability time to be incorrectly displayed on the Reagent Status screen with a status of "OK". In this scenario, the expired reagent will remain in the carousel for sample processing. 2) Performing monthly maintenance procedure 5701 Clean ICT Drain Tip incorrectly may potentially cause issues such as damaged connector or leaking connection. 3) A sample exception with message code 150 "Unable to process test. Previous processing module error" is produced without notifying the operator of a reagent pipettor failure and may cause processing module to transition into the Pausing state. Tests initiated prior to the sample exception may continue to process without dispense of reagents, potentially leading to incorrect results. 4. Reagent short dispense: Alinity c needs a control measure to protect against the potential for short reagent dispense. Addition of a maximum depth limit for reagent cartridges on the Alinity c to prevent the potential for a short dispense is needed. 5. RSM indicators were blinking green incorrectly: The Reagent and Sample Manager (RSM) indicators will incorrectly blink green indicating that processing is completed and the rack or cartridge can be removed from the loading area when the rack or cartridge should not be accessed. 6. Erroneous ICT Calibration Curves: Erroneous ICT calibration curves might be generated for the Alinity c when there is a malfunction of ICT reference solution delivery, use of wrong/evaporated calibrator, defective ICT modules, etc.

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

Recall #:
88502
Lot/product code:
Model Number: LN 03R70-01 all units with software versions 3.2.3 and earlier. Serial Numbers manufactured by Sanmina: SCM01001; SCM01002; SCM01003; SCM01004; SCM01005; SCM01006; SCM01007; SCM01008; SCM01009; SCM01010; SCM01011; SCM01012; SCM01013; SCM01014; SCM01015; SCM01016; SCM01017; SCM01018; SCM01019; SCM01020; SCM01021; SCM01022; SCM01023; SCM01024; SCM01025; SCM01026; SCM01027; SCM01028; SCM01029; SCM01030; SCM01031; SCM01032; SCM01033; SCM01034; SCM01035; SCM01036; SCM01037; SCM01038; SCM01039; SCM01040; SCM01041; SCM01042; SCM01043; SCM01044; SCM01045; SCM01046; SCM01047; SCM01048; SCM01049; SCM01050; SCM01051; SCM01052; SCM01053; SCM01054; SCM01055; SCM01056; SCM01057; SCM01058; SCM01059; SCM01060; SCM01061; SCM01062; SCM01063; SCM01064; SCM01065; SCM01066; SCM01067; SCM01068; SCM01069; SCM01070; SCM01071; SCM01072; SCM01073; SCM01074; SCM01075; SCM01076; SCM01077; SCM01078; SCM01079; SCM01080; SCM01081; SCM01082; SCM01083; SCM01084; SCM01085; SCM01086; SCM01087; SCM01088; SCM01089; SCM01090; SCM01091; SCM01092; SCM01093; SCM01094; SCM01095; SCM01096; SCM01097; SCM01098; SCM01099; SCM01100; SCM01101; SCM01102; SCM01103; SCM01104; SCM01105; SCM01106; SCM01107; SCM01108; SCM01109; SCM01110; SCM01112; SCM01113; SCM01114; SCM01115; SCM01116; SCM01117; SCM01118; SCM01119; SCM01120; SCM01121; SCM01122; SCM01123; SCM01124; SCM01125; SCM01126; SCM01127; SCM01128; SCM01129; SCM01130; SCM01131; SCM01132; SCM01133; SCM01134; SCM01135; SCM01136; SCM01137; SCM01138; SCM01139; SCM01140; SCM01141; SCM01142; SCM01143; SCM01144; SCM01145; SCM01146; SCM01147; SCM01148; SCM01149; SCM01150; SCM01151; SCM01152; SCM01153; SCM01154; SCM01155; SCM01156; SCM01157; SCM01158; SCM01159; SCM01160; SCM01161; SCM01162; SCM01163; SCM01164; SCM01165; SCM01166; SCM01167; SCM01168; SCM01169; SCM01170; SCM01171; SCM01172; SCM01173; SCM01174; SCM01175; SCM01176; SCM01177; SCM01178; SCM01179; SCM01180; SCM01181; SCM01182; SCM01183; SCM01184; SCM01185; SCM01186; SCM01187; SCM01188; SCM01189; SCM01190; SCM01191; SCM01192; SCM01193; SCM01194; SCM01195; SCM01196; SCM01197; SCM01198; SCM01199; SCM01200; SCM01201; SCM01202; SCM01203; SCM01204; SCM01205; SCM01206; SCM01207; SCM01208; SCM01209; SCM01210; SCM01211; SCM01212; SCM01213; SCM01214; SCM01215; SCM01216; SCM01217; SCM01218; SCM01219; SCM01220; SCM01221; SCM01222; SCM01223; SCM01224; SCM01225; SCM01226; SCM01227; SCM01228; SCM01229; SCM01230; SCM01231; SCM01232; SCM01234; SCM01235; SCM01236; SCM01237; SCM01238; SCM01239; SCM01240; SCM01241; SCM01242; SCM01243; SCM01244; SCM01245; SCM01246; SCM01247; SCM01248; SCM01249; SCM01250; SCM01251; SCM01252; SCM01253; SCM01254; SCM01255; SCM01256; SCM01257; SCM01258; SCM01259; SCM01260; SCM01261; SCM01262; SCM01263; SCM01264; SCM01265; SCM01266; SCM01267; SCM01268; SCM01269; SCM01270; SCM01271; SCM01272; SCM01273; SCM01274; SCM01275; SCM01276; SCM01277; SCM01278; SCM01279; SCM01280; SCM01281; SCM01282; SCM01283; SCM01284; SCM01285; SCM01286; SCM01287; SCM01288; SCM01289; SCM01290; SCM01291; SCM01292; SCM01293; SCM01294; SCM01295; SCM01296; SCM01297; SCM01298; SCM01299; SCM01300; SCM01301; SCM01302; SCM01303; SCM01304; SCM01305; SCM01306; SCM01307; SCM01308; SCM01309; SCM01310; SCM01311; SCM01312; SCM01313; SCM01314; SCM01315; SCM01316; SCM01317; SCM01318; SCM01319; SCM01320; SCM01321; SCM01322; SCM01323; SCM01324; SCM01325; SCM01326; SCM01327; SCM01328; SCM01329; SCM01330; SCM01331; SCM01332; SCM01333; SCM01334; SCM01335; SCM01336; SCM01337; SCM01338; SCM01339; SCM01340; SCM01341; SCM01342; SCM01343; SCM01344; SCM01345; SCM01346; SCM01347; SCM01348; SCM01349; SCM01350; SCM01351; SCM01352; SCM01353; SCM01354; SCM01355; SCM01356; SCM01357; SCM01358; SCM01359; SCM01360; SCM01361; SCM01362; SCM01363; SCM01364; SCM01365; SCM01366; SCM01367; SCM01368; SCM01369; SCM01370; SCM01371; SCM01372; SCM01373; SCM01374; SCM01375; SCM01376; SCM01377; SCM01378; SCM01379; SCM01380; SCM01381; SCM01382; SCM01383; SCM01384; SCM01385; SCM01386; SCM01387; SCM01388; SCM01389; SCM01390; SCM01391; SCM01392; SCM01393; SCM01394; SCM01395; SCM01396; SCM01397; SCM01399; SCM01400; SCM01401; SCM01402; SCM01403; SCM01404; SCM01405; SCM01406; SCM01407; SCM01408; SCM01409; SCM01410; SCM01411; SCM01412; SCM01413; SCM01414; SCM01415; SCM01416; SCM01417; SCM01418; SCM01419; SCM01420; SCM01421; SCM01422; SCM01423; SCM01424; SCM01425; SCM01426; SCM01427; SCM01428; SCM01429; SCM01430; SCM01431; SCM01432; SCM01433; SCM01434; SCM01435; SCM01436; SCM01437; SCM01438; SCM01439; SCM01440; SCM01441; SCM01442; SCM01443; SCM01444; SCM01445; SCM01446; SCM01447; SCM01448; SCM01449; SCM01450; SCM01451; SCM01452; SCM01453; SCM01454; SCM01455; SCM01456; SCM01457; SCM01458; SCM01459; SCM01460; SCM01461; SCM01462; SCM01463; SCM01464; SCM01465; SCM01466; SCM01467; SCM01468; SCM01469; SCM01470; SCM01471; SCM01472; SCM01473; SCM01474; SCM01475; SCM01476; SCM01477; SCM01478; SCM01479; SCM01480; SCM01481; SCM01482; SCM01483; SCM01484; SCM01485; SCM01486; SCM01487; SCM01488; SCM01489; SCM01490; SCM01491… (truncated, 53936 characters total — see the official FDA record for the full value)
Recalling firm:
Abbott Laboratories
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled July 27, 2021

REF TIN3015, 15G x 79 mm Bone Marrow Aspiration/Intraosseous Infusion Needle, For Single Use Only, Sterile EO, UDI: 10885403043796

Potential for needle protector to become fully dislodge exposing infusion needle which could result in needle stick.

ALL 50 STATES
▸Full report

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

Recall #:
88473
Lot/product code:
Lot/Serial Number - Exp. Date: 963162 6/30/2021; 967672 6/30/2021; 978229 7/31/2021; 986594 7/31/2021; 988075 7/31/2021; 991067 8/31/2021; 994373 8/31/2021; 996570 8/31/2021; 998004 8/31/2021; 998332 8/31/2021; 1000061 8/31/2021; 1004858 9/30/2021; 1005204 9/30/2021; 1007650 9/30/2021; 1010791 9/30/2021; 1013939 9/30/2021; 1017379 10/31/2021; 1035580 11/30/2021; 1035581 11/30/2021; 1038740 11/30/2021; 1044131 12/31/2021; 1049259 12/31/2021; 1050881 12/31/2021; 1052628 12/31/2021; 1057742 1/31/2022; 1059045 1/31/2022; 1061515 1/31/2022; 1065338 1/31/2022; 1066413 1/31/2022; 1066484 1/31/2022; 1068754 2/28/2022; 1069385 2/28/2022; 1072036 2/28/2022; 1072932 2/28/2022; 1076214 2/28/2022; 1078134 2/28/2022; 1078406 2/28/2022; 1080547 2/28/2022; 1082456 2/28/2022; 1085984 3/31/2022; 1086606 3/31/2022; 1087768 3/31/2022; 1088480 3/31/2022; 1089329 3/31/2022; 1089500 3/31/2022; 1090412 3/31/2022; 1092057 3/31/2022; 1094384 3/31/2022; 1095382 4/30/2022; 1097231 4/30/2022; 1097282 4/30/2022; 1098267 4/30/2022; 1099427 4/30/2022; 1102009 4/30/2022; 1109455 5/31/2022; 1110142 5/31/2022; 1112821 5/31/2022; 1113754 5/31/2022; 1116187 5/31/2022; 1121054 5/31/2022; 1122273 6/30/2022; 1125711 6/30/2022; 1125917 6/30/2022; 1127492 6/30/2022; 1127964 6/30/2022; 1129544 6/30/2022; 1130696 6/30/2022; 1132694 6/30/2022; 1137174 7/31/2022; 1138050 7/31/2022; 1142149 7/31/2022; 1143470 7/31/2022; 1143855 7/31/2022; 1144660 7/31/2022; 1146743 7/31/2022; 1150183 8/31/2022; 1151530 8/31/2022; 1152049 8/31/2022; 1152438 8/31/2022; 1153264 8/31/2022; 1155379 8/31/2022; 1155518 8/31/2022; 1155992 8/31/2022; 1158661 8/31/2022; 1159859 8/31/2022; 1161713 9/30/2022; 1164223 9/30/2022; 1166044 9/30/2022; 1167036 9/30/2022; 1167227 9/30/2022; 1167956 9/30/2022; 1169993 9/30/2022; 1180039 10/31/2022; 1189176 11/30/2022; 1190023 11/30/2022; 1190032 11/30/2022; 1194421 11/30/2022; 1194422 11/30/2022; 1198084 12/31/2022; 1198085 12/31/2022; 1200458 12/31/2022; 1200657 12/31/2022; 1202859 12/31/2022; 1204663 12/31/2022; 1206730 12/31/2022; 1209231 12/31/2022; 1210383 1/31/2023; 1210987 1/31/2023; 1213059 1/31/2023; 1214083 1/31/2023; 1214808 1/31/2023; 1217214 2/28/2023; 1218641 2/28/2023; 1220580 2/28/2023; 1221532 2/28/2023; 1230001 3/31/2023; 1234242 4/30/2023; 1234866 4/30/2023; 1237066 4/30/2023; 1239250 4/30/2023; 1241484 5/31/2023; 1243238 5/31/2023; 1245024 5/31/2023; 1250142 6/30/2023; 1253967 7/31/2023; 1255153 7/31/2023; 1256826 7/31/2023; 1257665 7/31/2023; 1260624 8/31/2023; 1261698 8/31/2023; 1263690 8/31/2023; 1268443 9/30/2023; 1269717 9/30/2023; 1276374 11/30/2023; 1276474 11/30/2023; 1277076 11/30/2023; 1277078 11/30/2023; 1278052 11/30/2023; 1279629 12/31/2023; 1280551 12/31/2023; 1281423 12/31/2023; 1282441 12/31/2023; 1282566 12/31/2023; 1285959 1/31/2024; 1289325 1/31/2024; 1290116 2/29/2024; 1290526 2/29/2024; 1290901 2/29/2024; 1291368 2/29/2024; 1291991 2/29/2024; 1293285 2/29/2024; 1293713 2/29/2024; 1294738 3/31/2024; 1296369 3/31/2024; 1297347 3/31/2024; 1298132 3/31/2024; 1299347 4/30/2024; 1302001 4/30/2024; 1302770 4/30/2024; 1304508 4/30/2024; 1305180 5/31/2024; 1306210 5/31/2024; 1306618 6/30/2024; 1307348 5/31/2024; 1308370 5/31/2024; 1309271 6/30/2024; 1310700 6/30/2024; 1312765 6/30/2024; 1313035 6/30/2024; 1313638 6/30/2024; 1315612 7/31/2024; 1319007 8/31/2024; 1321484 8/31/2024; 1321909 8/31/2024; 1323424 9/30/2024; 1324561 9/30/2024; 1325914 9/30/2024; 1326666 9/30/2024; 1328546 10/31/2024; 1328868 10/31/2024; 1330383 10/31/2024; 1331229 11/30/2024; 1334317 11/30/2024; 1335560 11/30/2024; 1336948 12/31/2024; 1346946 2/28/2025; 1350086 2/28/2025; 1352112 2/28/2025; 1353076 2/28/2025; 1354658 3/31/2025; 1355795 3/31/2025; 1356579 3/31/2025; 1364166 5/31/2025; 1370390 6/30/2025; 1371002 6/30/2025; 1372716 6/30/2025; 1372717 6/30/2025; 1373632 6/30/2025; 1374321 6/30/2025; 1374720 6/30/2025; 1376484 7/31/2025; 1376558 7/31/2025; 1378293 7/31/2025; 1379114 7/31/2025; 1379319 7/31/2025; 1379975 7/31/2025; 1380313 7/31/2025; 1382427 8/31/2025; 1382905 8/31/2025; 1383730 8/31/2025; 1384557 8/31/2025; 1389054 9/30/2025; 1389688 9/30/2025; 1389835 9/30/2025; 1390329 10/31/2025; 1392449 10/31/2025; 1392925 10/31/2025; 1393712 10/31/2025; 1395327 11/30/2025; 1396203 11/30/2025; 1397019 11/30/2025; 1397577 11/30/2025; 1397579 11/30/2025; 1399709 12/31/2025; 1401245 1/31/2026; 1402635 1/31/2026; 1403128 1/31/2026; 1404960 1/31/2026; 1405506 1/31/2026; 1408600 2/28/2026; 1409355 2/28/2026; 1411640 3/31/2026; 1412991 3/31/2026; 1414301 4/30/2026; 1414832 4/30/2026; 1416059 4/30/2026; 1417013 4/30/2026; 1418166 4/30/2026; 1418927 5/31/2026; 1419365 5/31/2026; 1420607 5/31/2026
Recalling firm:
Bard Peripheral Vascular Inc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled July 28, 2021

Power Processor 3K, 3K High Speed Stockyards Module Nameplate: PP 3K Stockyard (Refrig) 9707 REF A88116

Missing splash guard which may expose users to hazardous materials. .

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▸Full report

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

Recall #:
88615
Lot/product code:
Catalog Number: A88116 - 3K HS Refrigerated Stockyard UDI: 15099590591960 Serial Numbers: 90HF1304006; 90HF1306009; 90HF1303005; 90HF1508005; 90HF1302005; 90HF1610005; 90HF1806001; 90HF1209005; 90HF1303007; 90HF1708006; 90HF1205001; 90HF1805002; 90HF1402005; 90HF1503001; 90HF1104002; 90HF1208004; 90HF1208005; 90HF1203001; 90HF1012004; 90HF1101002; 90HF1702003; 90HF1402004; 90HF1303008; 90HF1210001; 90HF1207001; 90HF1305007; 90HF1305004; 90HF1610001; 90HF1505002; 90HF1307005; 90HF1610002; 90HF1508003; 90HF1210002; 90HF1306001; 90HF1206002; 90HF1208002; 90HF1305008; 90HF1009002; 90HF1101001; Catalog Number: 6915556 - Power Processor 3K Stockyard (Stockyard 3000/R Kit for PWR PROC) Serial Numbers: 90AM0805001; 90AM0902009; 90AM0902005; 90AM0806003; 90AM0801003; 90AM0802002; 90AM0803001; 90AM0912002; 90AM1003002; 90AM0905010; 90AM0801004; 90AM06007008; 90AM060703; 90AM060704; 90AM0710002; 90AM0905007; 90AM0710008; 90AM0903002; 90AM0808002; 90AM0711004; 90AM0711005; 90AM0810001; 90AM0901002; 90AM0905006; 90AM0904004; 90AM0904005; 90AM0803002; 90AM0710004; Amended - additional Products and Codes (12/15/2021): B05520 - Stockyard, 5K HS, Refrigerated Serial Numbers: 90HG1104002; 90HG1101001; 90HG1105002; 90HG1104001; 90HG1101003; 90HG1101002; 90HG1202004; 90HG1102005; 90HG1101004; 90HG1206002; A88115 - 5K HS Refrig Stockyard Serial Numbers: 90HG0911001 90HG0911003 90HG0911002
Recalling firm:
Beckman Coulter Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled July 28, 2021

Accu-Chek Performa Test Strip, Blood Glucose Monitoring System, Model number 07299702001

Test strip vials may open while inside sealed cartons during shipment. An open vial might expose the test strips to humidity, which might damage the strips and result in inaccurate results, potentially leading to inappropriate therapy decisions and adverse health consequences.

ALL 50 STATES
▸Full report

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

Recall #:
88362
Lot/product code:
Since this is a labeling correction, this recall is not lot specific and is applicable to all non-expired lots.
Recalling firm:
Roche Diabetes Care, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled July 28, 2021

Accu-Chek Aviva Plus Test Strip, Blood Glucose Monitoring System, Model numbers: 06908152001, 06908217001, 06908268001, 06908349001, 06908373001

Test strip vials may open while inside sealed cartons during shipment. An open vial might expose the test strips to humidity, which might damage the strips and result in inaccurate results, potentially leading to inappropriate therapy decisions and adverse health consequences.

ALL 50 STATES
▸Full report

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

Recall #:
88362
Lot/product code:
Since this is a labeling correction, this recall is not lot specific and is applicable to all non-expired lots.
Recalling firm:
Roche Diabetes Care, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled July 28, 2021

Accu-Chek SmartView Test Strip, Blood Glucose Monitoring System, Model numbers: 06337538001, 06337546001, 06337562001

Test strip vials may open while inside sealed cartons during shipment. An open vial might expose the test strips to humidity, which might damage the strips and result in inaccurate results, potentially leading to inappropriate therapy decisions and adverse health consequences.

ALL 50 STATES
▸Full report

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

Recall #:
88362
Lot/product code:
Since this is a labeling correction, this recall is not lot specific and is applicable to all non-expired lots.
Recalling firm:
Roche Diabetes Care, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled July 28, 2021

Accu-Chek Inform II Test Strip, Whole Blood Glucose Test System, Model number 05942891001

Test strip vials may open while inside sealed cartons during shipment. An open vial might expose the test strips to humidity, which might damage the strips and result in inaccurate results, potentially leading to inappropriate therapy decisions and adverse health consequences.

ALL 50 STATES
▸Full report

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

Recall #:
88362
Lot/product code:
Since this is a labeling correction, this recall is not lot specific and is applicable to all non-expired lots.
Recalling firm:
Roche Diabetes Care, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled July 29, 2021

HANA/PROFx CLASSIC FEMORAL HOOK RIGHT REF 6850-144

One batch of "regular" femoral hooks were incorrectly etched with the "classic" femoral hook model number.

ALL 50 STATES
▸Full report

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

Recall #:
90603
Lot/product code:
Model Number: 6850-144 UDI Code: (01)00842430106842(10)MIZ210712(11)210712 Lot/Batch Number: MIZ210712
Recalling firm:
Mizuho OSI
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled July 29, 2021

Erythromycin Topical Solution USP, 2%, 60mL bottle, Rx only, Teligent Pharma, Inc. Buena, NJ 08310, NDC 52565-027-59

Defective container: possibility for lack of seal integrity.

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▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0769-2021
Lot/product code:
Lot #: 14892, Exp 1/2022
Recalling firm:
Teligent Pharma, Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled July 30, 2021

Combipatch (estradiol/norethindrone acetate transdermal system) 0.05/0.14 mg per day, 50/140 Twice Weekly, Rx Only a) 2 Systems NDC 68968-0514-2 b) 8 Systems NDC 68968-0514-8, Mfd. by: Noven Pharmaceuticals, Inc., Miami, Florida 33186, Dist. by: Noven Therapeutics LLC, Miami, Florida 33186

Failed Stability Specifications; not meeting quality requirements for shear.

ALL 50 STATES
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0724-2021
Lot/product code:
Lots: 88542 Exp. 03/2022; 88227 Exp. 12/2021; 88696 Exp. 05/2022; 89357 Exp. 08/2022
Recalling firm:
Noven Pharmaceuticals Inc
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled July 30, 2021

Combipatch (estradiol/norethindrone acetate transdermal system) 0.05/0.25 mg per day 50/250 Twice Weekly Rx Only a) 2 Systems NDC 68968-0525-2; b) 8 Systems NDC 68968-0525-8, Mfd. by: Noven Pharmaceuticals, Inc., Miami, Florida 33186, Dist. by: Noven Therapeutics LLC, Miami, Florida 33186

Failed Stability Specifications; not meeting quality requirements for shear.

ALL 50 STATES
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0725-2021
Lot/product code:
Lots: 88540 Exp. 03/2022; 89118 Exp. 05/2022; 89244 Exp. 07/2022; 89244 (sample lot) Exp. 07/2022
Recalling firm:
Noven Pharmaceuticals Inc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled August 2, 2021

BD SmartSite Bag Access Device Needle-Free Valve, REF: 2300E; BD Bag access Device with 1 Check Valve And Needle Free Valve, REF: 2309E-0006

Needle-free connector valves, either standalone or attached to extension sets, may have issues including difficulty to flush, flow issues, and partial or total occlusions, which could lead to therapy delay. Follow-up activates not required if product has already been used or was safely connected to the female luer of connecting device.

ALL 50 STATES
▸Full report

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

Recall #:
88203
Lot/product code:
Lots:  20066502 20066503 20066504 20076251 20076352 20086483 20086484 20086485 20086486 20087129 20087130 20096280 20096281 20096282 20096283 20097163 20105074 20105075 20095374 20095375 20096302 20105754 20105755 20105756 20105757 20105758 20115470 21036462 21036463 21036464 21036465 21036466
Recalling firm:
CAREFUSION
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled August 2, 2021

BD Extension Set SMALLBORE Tubing with 2 SmartSite VALVES, REF: 20019E

Needle-free connector valves, either standalone or attached to extension sets, may have issues including difficulty to flush, flow issues, and partial or total occlusions, which could lead to therapy delay. Follow-up activates not required if product has already been used or was safely connected to the female luer of connecting device.

ALL 50 STATES
▸Full report

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

Recall #:
88203
Lot/product code:
UDI: 27613203013813; Lots: 21045673 21045672 21045671 21045670 21045669 21045243 21036889 21036844 21036767 21036766 21036698 21036697 21036696 21036695 21036643 21036642 21026547 21026546 21026545 21026379 21026378 21026377 21026327 21026326 21026325 21026324 21026323 21025283 21025282 21025281 21025280 21025279 21025278 21025157 21025156 21025155 21016751 21016394 21016393 21015306 21015305 20126555 20126554 20126553 20126552 20126529 20126528 20126527 20126526 20125986 20125985 20125984 20125983 20125982 20125981 20125980 20125979 20125978 20125977 20125976 20125975 20125974 20125973 20125972 20125950 20125949 20125948 20115023 20115022 20115021 20115020 20115019 20115018 20115017 20115016 20115015 20115014 20106570 20106231 20106230 20106229 20105085 20105084 20095138 20095137 20095136 20095135 20095134 20095133 20095132 20066719 20066718 20066717 20066448 20066447 20066446 20066231 20066230 20066229 20066228 20066109 20066108 20066107 20066106 20066105 20066104 20055332 20055331 20055330 20055329 20055080 20055079 20055078 20055077 20055076 20045843 20045842 20045841 20045840 20045839 20045838 20045837 20045836 20035578 20035577 20035496 20035495 20035494 20035493 20025024 20025023 20025022 20025021 20016446 20016445 20016444 20016443 20016442 20016317 20016316 20016315 20016194 20016193 20016192 20016191 20016190 20016105 20016104
Recalling firm:
CAREFUSION
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