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Recalls affecting District of Columbia

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

16,249 recalls found

Just announced

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

Business Pill, Branch Manager for Mendietary supplements marketed for male sexual enhancement

Products contain undeclared yohimbine

Full report
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 AliveMoringa Leaf Powder

Potential to be contaminated with Salmonella

Full report
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. Braun0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container

Presence of particulate matter identified as iron oxide

Full report
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 ValueOrganic Triple Berry Blend

Possible E. Coli Contamination

Full report
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

Full report
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 TemptationsChocolatey Eyeballs, 7 oz., 10 oz., 10.5 oz., 11 oz., and 16 oz.

Undeclared milk

Full report
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

LipofitLipofit Extreme 2.0 Fat Burner Dietary Supplement

Undeclared Fluoxetine and 2,4-Dinitrophenol (DNP)

Full report
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

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

KofinasGarlic Mediterranean Infused Extra Virgin Olive Oil 500 ml, 250 ml, and 100 ml

Contains garlic essential oil not approved for culinary use

Full report
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 SproutsRobust Radish Mix, 5oz Cups

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

Full report
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

MartinaMangoes

Potential contamination with Salmonella

Full report
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 September 22, 2021

ProxiDiagnost N90 is multi-functional general R/F systems.

The Aleva monitor requires certain labels to be applied, some of which are required by FDA Electronic Product Radiation Control performance standards. This includes the Radiation Warning Label [21CFR 1020.30 (j)] and the X-ray control certification statement [21 CFR 1010.2]. Philips has determined that some systems at customer locations did not have these labels applied.

ALL 50 STATES
Full report

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

Recall #:
89023
Lot/product code:
ProxiDiagnost N90
Recalling firm:
Philips Healthcare
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled September 22, 2021

VIDAS Lyme IgM II (LYM), REF 416436

BioMerieux has been receiving an increasing number of complaints linked to a VIDAS substrate error. It prevents the test from being run, therefore leads to potential delayed results as the user must run another test.

ALL 50 STATES
Full report

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

Recall #:
88797
Lot/product code:
UDI 03573026447151, Lot #: 1008636750, 1008768920, 1008857410
Recalling firm:
bioMerieux, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled September 22, 2021

VIDAS Lyme IgG II (LYM), REF 417401

BioMerieux has been receiving an increasing number of complaints linked to a VIDAS substrate error. It prevents the test from being run, therefore leads to potential delayed results as the user must run another test.

ALL 50 STATES
Full report

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

Recall #:
88797
Lot/product code:
UDI 03573026458270, Lot #: 1008714880, 1008824220
Recalling firm:
bioMerieux, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled September 23, 2021

Clinician Programmer Application (CPA) model A610 Clinician Software Application

A software anomaly may occur with the clinician programmer application.

ALL 50 STATES
Full report

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

Recall #:
88761
Lot/product code:
Clinician Programmer Application (CPA) model A610 version 3.0.1048, 3.0.1057, 3.0.1062, and 3.0.1081
Recalling firm:
Medtronic Neuromodulation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled September 23, 2021

ImplantDirect, REF 834713, Legacy 2 Implant 4.7mmD x 13mmL, 4.5mmD Platform,

Packaged dental implant contains a different size then the size declared on the labeling.

ALL 50 STATES
Full report

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

Recall #:
88859
Lot/product code:
lot # 166300 / UDI: 10841307101796
Recalling firm:
Implant Direct Sybron Manufacturing LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled September 23, 2021

SIMPLEXA COVID-19 Positive Control Pack, REF MOL4160, IVD, Rx Only, UDI: (01) 20816101027051

Due to unapproved raw materials used in the manufacturing of Covid-19 control pack, their is the potential for delayed amplification signals.

ALL 50 STATES
Full report

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

Recall #:
88825
Lot/product code:
Lot #/Expiration Date: 12175N/11.30.2021, 12722N/01.31.2022, X12122N/01.31.2022, X12724N/08.31.2022
Recalling firm:
DiaSorin Molecular LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled September 23, 2021

ImplantDirect, REF 834711, Legacy 2 Implant 4.7mmD x 11.5mmL, 4.5mmD Platform,

Packaged dental implant contains a different size then the size declared on the labeling.

ALL 50 STATES
Full report

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

Recall #:
88859
Lot/product code:
lot # 166297 / UDI: 10841307101789
Recalling firm:
Implant Direct Sybron Manufacturing LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled September 24, 2021

Artis zeego, Fluoroscopic X-Ray System Models: 10280959,10502505, 10848283 in combination with the following workplace/system application software models: Product/Model #: syngo X Workplace, 10281061 syngo X Workplace, 10281299 syngo X Workplace, 10502522 Syngo Application Software, 10848815

Software error, the software can produce an incorrect interpretation of the table rotation if the table has been rotated by more than 4degrees in either direction. This can cause the 3D image reconstruction to be shown rotated by up to 5 degrees relative to the patient and to be used inappropriately by the system and result in incorrect treatment of the patient

ALL 50 STATES
Full report

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

Recall #:
88820
Lot/product code:
Artis zeego systems with Artis patient table and AppSW VD20C/VD20N
Recalling firm:
Siemens Medical Solutions USA, Inc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled September 24, 2021

Permobil TiLite, Models: Aero Z, and ZRA

Some affected wheelchairs, with transit tie downs, that are used as a passenger seat in a motor vehicle may not be configured in the right orientation to perform as intended if involved in a motor vehicle accident. Some affected wheelchairs can no longer be used as a passenger seat until transit tie downs are replaced with redesigned transit tie downs, verified, and released to the market.

ALL 50 STATES
Full report

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

Recall #:
88718
Lot/product code:
Manufactured between January 19, 2017 and June 14, 2021 with the serial number range from M2005054 to 1231112011
Recalling firm:
TiSport, Llc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled September 24, 2021

Philips Azurion systems with software releases 2.1(L1) and 2.1(L2)

3D-RA is a reconstruction software product that can be used with the Philips Azurin system. This product extends the functionality of compatible X-ray equipment with the capability of 3D X-ray imaging. Before starting a 3D-RA scan, the detector of the Philips Azurion system must be positioned in portrait or landscape orientation with an angle of 0 or +/-90 degrees relative to the 3D scan direction. Philips has discovered that Azurion releases 2.1(L1) and 2.1(L2) allow creation of a 3D-RA scan with a deviating detector orientation of up to 3 degrees from the exact portrait or landscape orientation (i.e., at 0 or +/-90 degrees), relative to the 3D scan direction. 3D-RA scans with a deviating detector orientation of ore than 1.0 degree from the exact portrait or landscape orientation (i.e., at 0 or +/-90 degrees) cannot be reconstructed with the 3D-RA reconstruction software.

ALL 50 STATES
Full report

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

Recall #:
89020
Lot/product code:
Azurion 2.1(L1) and 2.1(L2)
Recalling firm:
Philips Healthcare
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled September 27, 2021

HALYARD STERLING ZERO NITRILE POWDER-FREE EXAM GLOVES, Sizes XS, S, M, L, and XL

All lots of the glove may discolor and lose elasticity upon aging, resulting in the inability of the user to don the gloves without tearing.

ALL 50 STATES
Full report

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

Recall #:
88846
Lot/product code:
All lots of the following sizes: a. XS, REF 47459, UDI (01)20680651474593 b. S, REF 47460, UDI (01)20680651474609 c. M, REF 47461, UDI (01)20680651474616 d. L, REF 47462, UDI (01)20680651474623 e. XL, REF 47463, UDI (01)20680651474630
Recalling firm:
O&M HALYARD INC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled September 28, 2021

Atellica IM 1300 Analyzer, SMN 11066001

Ancillary reagent packs used on Atellica IM 1300 and Atellica IM 1600 analyzers may overflow when pierced while on an analyzer located at an altitude of greater than 350m (1148ft) above sea level. As a result, customers at these altitudes may observe an increased number of Reagent Volume Check Errors.

ALL 50 STATES
Full report

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

Recall #:
88792
Lot/product code:
All units
Recalling firm:
Siemens Healthcare Diagnostics, Inc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled September 28, 2021

Atellica IM 1600 Analyzer, SMN 11066000

Ancillary reagent packs used on Atellica IM 1300 and Atellica IM 1600 analyzers may overflow when pierced while on an analyzer located at an altitude of greater than 350m (1148ft) above sea level. As a result, customers at these altitudes may observe an increased number of Reagent Volume Check Errors.

ALL 50 STATES
Full report

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

Recall #:
88792
Lot/product code:
All units.
Recalling firm:
Siemens Healthcare Diagnostics, Inc
View official FDA record (opens in a new tab)
Class IIILow risk
DrugRecalled September 28, 2021

Butalbital, APAP, Caf 50/325/40 Tablet, packaged in a) 12-count bottles, NDC: 71335-1767-09, barcode 083929164865; b) 20-count bottles, NDC: 71335-1767-01, barcode 083921157837; c) 30-count bottles, NDC: 71335-1767-02, barcode 083922165687, d) 60-count bottles, NDC: 71335-1767-03, barcode 083923153776, e) 90-count bottles, NDC: 71335-1767-04, barcode 083924152889, f) 120-count bottles, NDC: 71335-1767-07, barcode 083927153735. Westminster Pharmaceuticals LLC, Rx only, Packaged by Bryant Ranch Prepack, Burbank, CA 91504 USA

Labeling: Not Elsewhere Classified: the controlled substance classification "CIII" is missing on the label

ALL 50 STATES
Full report

A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.

Recall #:
D-0257-2022
Lot/product code:
a) Lots: 164865, Exp: 2/28/2021; 162113, Exp: 8/31/2022; 160419, Exp: 2/28/2023; 160004, 155752, 154380, 153776, 152889, Exp: 8/31/2022, b) Lots: 157837, 154997, Exp: 8/31/2022, c) Lots: 165687, 160419, 160330, Exp: 2/28/2023; 159973, 159943, 159352, 159345, 158841, 155752, 152347, Exp: 8/31/2022; 152245, 152156, 152197, 151338, 151160, Exp: 7/31/2022, d) Lots: 162641, Exp: 2/28/2023; 154380, 153776, 152889, Exp: 8/31/2022, e)Lots: 158841, 152889, Exp: 8/31/2022, f) Lots: 153776, 153735, 152347, Exp: 8/31/2022
Recalling firm:
Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals
View official FDA record (opens in a new tab)
Class IIILow risk
DrugRecalled September 28, 2021

Butalbital, APAP, Caf 50/325/40 Tablets, packaged in a) 12-count bottles, NDC: 63629-8392-09, barcode 083929152151; b) 60-count bottles, NDC: 63629-8392-03, barcode 083923152614; c) 90-count bottles, NDC:63629-8392-04, barcode 083924152614, Lannett Company Inc; Rx only, Packaged by Bryant Ranch Prepack, Burbank, CA 91504.

Labeling: Not Elsewhere Classified: the controlled substance classification "CIII" is missing on the label

ALL 50 STATES
Full report

A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.

Recall #:
D-0256-2022
Lot/product code:
a) Lots: 152838, 152156, 152151, 151708, 151693, 151375, 151131, 151114, Exp: 7/31/2022, b) Lots: 152245, 151822, 151708, 151160, 151131, Exp: 7/31/2022, c) Lot #: 152614, Exp: 7/31/2022.
Recalling firm:
Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled September 28, 2021

The Natural Dentist Healthy Balance Peppermint Sage, Menthol 0.12%, 16.9 FL OZ (500 mL) bottles, Manufactured for Revive Personal Products Company, Madison, NJ 07940, UPC 7 14132 00071 4

Labeling; Label mix-up and Wrong Bar Code; back label incorrectly states active ingredient as Menthol with UPC 7 14132 00071 4 instead of Peppermint Oil and Sage Oil with UPC 7 14132 00073 8

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-0364-2022
Lot/product code:
Lot 2091A, exp 7/2023
Recalling firm:
Revive Personal Products Company
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled September 29, 2021

LEEP PRECISION Integrated System, 120V CooperSurgical part number: LP-10-120

Coagulate function may not operate with the use of the Hand Switch, failure of the device to coagulate tissue may lead to a prolonged procedure requiring medical intervention to control any intraoperative bleeding and complete the case.

ALL 50 STATES
Full report

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

Recall #:
88648
Lot/product code:
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(truncated, 17167 characters total — see the official FDA record for the full value)
Recalling firm:
CooperSurgical, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled September 29, 2021

ARCHITECT i1000SR REF 01L86-01/1L86 and 1L87; ARCHITECT i2000SR REF 03M74-02/3M74; ARCHITECT i2000 REF 08C89-01/1G17 and 8C89

Twelve software-related issues affecting software version 9.41 and earlier were identified. The issues include bypassing error codes, incorrect calibration, loss of module communication leading to overfilling wash buffer containers, missing QC flags, signal spikes, abnormal optics reads, and incorrect sample aspiration. The issues may lead to inaccurate results with an unknown bias direction and magnitude for assays measuring cardiac, metabolic (including diabetes), toxicology, prenatal, therapeutic drug monitoring, infectious disease, oncology, hepatic, pancreatic, hematological, endocrinologic, inflammatory analytes.

Full report

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

Recall #:
88880
Lot/product code:
Product Description/List Number/Serial Numbers: ARCHITECT i1000SR UDI: (01)00380740001537(21)I1SR12345(240)01L8601 List Number: 1L86 Serial Numbers: i1SR00101 i1SR00102 i1SR00103 i1SR00104 i1SR00105 i1SR00106 i1SR00107 i1SR00108 i1SR00109 i1SR00110 i1SR00111 i1SR00112 i1SR00113 i1SR00114 i1SR00115 i1SR00116 i1SR00117 i1SR00118 i1SR00119 i1SR00120 i1sr00121 i1SR00122 i1SR00124 i1SR00201 i1SR00202 i1SR00203 i1SR00204 i1SR00205 i1SR00206 i1SR00207 i1SR00208 i1SR00209 i1SR00210 i1SR00211 i1SR00212 i1SR00213 i1SR00214 i1SR00215 i1SR00216 i1SR00217 i1SR00218 i1SR00219 i1SR00220 i1SR00221 i1SR00222 i1SR00223 i1SR00224 i1SR00225 i1SR00226 i1SR00227 i1SR00228 i1SR00229 i1SR00230 i1SR00231 i1SR00232 i1SR00233 i1SR00234 i1SR00235 i1SR00236 i1SR00237 i1SR00238 i1SR00239 i1SR00240 i1SR00241 i1SR00242 i1SR01001 i1SR01002 i1SR01003 i1SR01004 i1SR01005 i1SR01006 i1SR01007 i1SR01008 i1SR01009 i1SR01010 i1SR01011 i1SR01012 i1SR01013 i1SR01014 i1SR01015 i1SR01016 i1SR01017 i1SR01018 i1SR01019 i1SR01020 i1SR01021 i1SR01022 i1SR01023 i1SR01024 i1SR01025 i1SR01026 i1SR01027 i1SR01028 i1SR01029 i1SR01030 i1SR01031 i1SR01032 i1SR01033 i1SR01034 i1SR01035 i1SR01036 i1SR01037 i1SR01038 i1SR01039 i1SR01040 i1SR01041 i1SR01042 i1SR01043 i1SR01044 i1SR01045 i1SR01046 i1SR01047 i1SR01048 i1SR01049 i1SR01050 i1SR01051 i1SR01052 i1SR01053 i1SR01054 i1SR01055 i1SR01056 i1SR01058 i1SR01059 i1SR01060 i1SR01061 i1SR01062 i1SR01063 i1SR01064 i1SR01065 i1SR01066 i1SR01067 i1SR01068 i1SR01069 i1SR01070 i1SR01071 i1SR01072 i1SR01073 i1SR01074 i1SR01075 i1SR01076 i1SR01077 i1SR01078 i1SR01079 i1SR01080 i1SR01082 i1SR01083 i1SR01084 i1SR01085 i1SR01086 i1SR01087 i1SR01088 i1SR01089 i1SR01090 i1SR01091 i1SR01092 i1SR01093 i1SR01094 i1SR01095 i1SR01096 i1SR01097 i1SR01098 i1SR01099 i1SR01100 i1SR01101 i1SR01102 i1SR01103 i1SR01104 i1SR01105 i1SR01106 i1SR01107 i1SR01108 i1SR01109 i1SR01110 i1SR01111 i1SR01112 i1SR01113 i1SR01114 i1SR01115 i1SR01116 i1SR01117 i1SR01118 i1SR01119 i1SR01120 i1SR01121 i1SR01122 i1SR01123 i1SR01124 i1SR01125 i1SR01126 i1SR01127 i1SR01128 i1SR01129 i1SR01130 i1SR01131 i1SR01132 i1SR01133 i1SR01134 i1SR01136 i1SR01137 i1SR01138 i1SR01139 i1SR01140 i1SR01141 i1SR01142 i1SR01143 i1SR01144 i1SR01145 i1SR01146 i1SR01147 i1SR01148 i1SR01149 i1SR01150 i1SR01151 i1SR01152 i1SR01153 i1SR01154 i1SR01155 i1SR01156 i1SR01157 i1SR01158 i1SR01159 i1SR01160 i1SR01161 i1SR01162 i1SR01163 i1SR01164 i1SR01165 i1SR01166 i1SR01167 i1SR01168 i1SR01169 i1SR01170 i1SR01171 i1SR01172 i1SR01173 i1SR01174 i1SR01175 i1SR01176 i1SR01177 i1SR01178 i1SR01179 i1SR01180 i1SR01181 i1SR01182 i1SR01183 i1SR01184 i1SR01185 i1SR01186 i1SR01187 i1SR01188 i1SR01189 i1SR01190 i1SR01191 i1SR01192 i1SR01193 i1SR01194 i1SR01195 i1SR01196 i1SR01197 i1SR01198 i1SR01199 i1SR01200 i1SR01201 i1SR01202 i1SR01203 i1SR01204 i1SR01205 i1SR01206 i1SR01207 i1SR01208 i1SR01209 i1SR01210 i1SR01211 i1SR01212 i1SR01213 i1SR01214 i1SR01215 i1SR01216 i1SR01217 i1SR01218 i1SR01219 i1SR01220 i1SR01221 i1SR01222 i1SR01223 i1SR01224 i1SR01225 i1SR01226 i1SR01227 i1SR01228 i1SR01229 i1SR01230 i1SR01231 i1SR01232 i1SR01233 i1SR01234 i1SR01235 i1SR01236 i1SR01237 i1SR01238 i1SR01239 i1SR01240 i1SR01241 i1SR01242 i1SR01243 i1SR01244 i1SR01245 i1SR01246 i1SR01247 i1SR01248 i1SR01249 i1SR01250 i1SR01251 i1SR01252 i1SR01253 i1SR01254 i1SR01255 i1SR01256 i1SR01257 i1SR01258 i1SR01259 i1SR01260 i1SR01261 i1SR01262 i1SR01263 i1SR01264 i1SR01265 i1SR01266 i1SR01267 i1SR01268 i1SR01269 i1SR01270 i1SR01271 i1SR01272 i1SR01273 i1SR01274 i1SR01275 i1SR01276 i1SR01277 i1SR01278 i1SR01279 i1SR01280 i1SR01281 i1SR01282 i1SR01283 i1SR01284 i1SR01285 i1SR01286 i1SR01287 i1SR01288 i1SR01289 i1SR01290 i1SR01291 i1SR01292 i1SR01293 i1SR01294 i1SR01295 i1SR01296 i1SR01297 i1SR01298 i1SR01299 i1SR01300 i1SR01301 i1SR01302 i1SR01303 i1SR01304 i1SR01305 i1SR01306 i1SR01308 i1SR01309 i1SR01310 i1SR01311 i1SR01312 i1SR01313 i1SR01314 i1SR01315 i1SR01316 i1SR01317 i1SR01318 i1SR01319 i1SR01320 i1SR01321 i1SR01322 i1SR01323 i1SR01324 i1SR01325 i1SR01326 i1SR01327 i1SR01328 i1SR01329 i1SR01330 i1SR01331 i1SR01332 i1SR01333 i1SR01334 i1SR01335 i1SR01336 i1SR01337 i1SR01338 i1SR01339 i1SR01340 i1SR01341 i1SR01342 i1SR01343 i1SR01344 i1SR01345 i1SR01346 i1SR01347 i1SR01348 i1SR01349 i1SR01350 i1SR01351 i1SR01352 i1SR01353 i1SR01354 i1SR01355 i1SR01356 i1SR01357 i1SR01358 i1SR01359 i1SR01360 i1SR01361 i1SR01362 i1SR01363 i1SR01364 i1SR01365 i1SR01366 i1SR01367 i1SR01368 i1SR01369 i1SR01370 i1SR01371 i1SR01372 i1SR01373 i1SR01374 i1SR01375 i1SR01376 i1SR01377 i1SR01378 i1SR01379 i1SR01380 i1SR01381 i1SR01382 i1SR01383 i1SR01384 i1SR01385 i1SR01386 i1SR01387 i1SR01388 i1SR01389 i1SR01390 i1SR01391 i1SR01392 i1SR01393 i1SR01394 i1SR01395 i1SR01396 i1SR01397 i1SR01398 i1SR01399 i1SR01400 i1SR01401 i1SR01402 i1SR01403 i1SR01404 i1SR01405 i1SR01406 i1SR01407 i1SR01408 i1SR01409 i1SR01410 i1SR01411 i1SR01412 i1SR01413 i1SR01414 i1SR01415 i1SR01416 i1SR01417 i1SR01418 i1SR01419 i1SR01420 i1SR01421 i1SR01422 i1SR01423 i1SR01424 i… (truncated, 311449 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 September 29, 2021

LEEP PRECISION Generator 120V Cooper Surgical Part Number: LP-20-120

Coagulate function may not operate with the use of the Hand Switch, failure of the device to coagulate tissue may lead to a prolonged procedure requiring medical intervention to control any intraoperative bleeding and complete the case.

ALL 50 STATES
Full report

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

Recall #:
88648
Lot/product code:
Serial Numbers:  0215002 1214007 2015050001  2016060030 2016060031 2016070002 2016070004 2016070012 2016070017 2016070021 2016070022 2016070026 2016070027 2016070028 2016070030 2016070031 2016080002 2016080004 2016080007 2016080009 2016080015 2016080016 2016080017 2016080018 2016080019 2016080020 2016080021 2016080022 2016080025 2016080026 2016080027 2016080029 2016080031 2016080033 2016080034 2016080035 2016080036 2016100002 2016100004 2016100009 2016100010 2016100012 2016100013 2016100014 2016100016 2016100017 2016100018 2016100021 2016100023 2016100024 2016100025 2016100027 2016100028  2015050016 2015050017 2015050018 2015050019 2015050020 2015110007 2016030001 2016030002 2016030006 2016030007 2016030013 2016030015 2016040001 2016040002 2016040004 2016040006 2016040007 2016040010 2016050004 2016050006 2016050007 2016050010 2016050012 2016050013 2016050015 2016050016 2016050019 2016050029 2016050031 2016050034 2016060001 2016060002 2016060003 2016060004 2016060006 2016060007 2016060009 2016060012 2016060013 2016060016 2016060021 2016060022 2016060023 2016060025 2016060026 2016060028 2016060029 2016100029 2016100033 2016100034 2016100035 2016120002 2016120003 2016120004 2016120005 2016120008 2016120010 2016120011 2017010001 2017010002 2017010003 2017010004 2017010005 2017010006 2017010007 2017010009 2017010010 2017010011 2017010012 2017010015 2017010016 2017010018 2017010020 2017010023 2017020001 2017020002 2017020003 2017020004 2017020005 2017020006 2017020008 2017020011 2017020012 2017020013 2017020014 2017020017 2017020019 2017040001 2017040002 2017040003 2017040005 2017040008 2017040015 2017050008 2017050012 2017050013 2017050014 2017050015 2017050016 2017050017 2017060003 2017060004 2017060006 2017060010 2017060011 2017060012 2017060013 2017060014 2017060015 2017070002 2017070003 2017070005 2017070006 2017070009 2017070010 2017070012 2017070013 2017070015 2017080001 2017080003 2017080004 2017080005 2017080007 2017080010 2017080011 2017080015 2017090001 2017090003 2017090006 2017090009 2017090010 2017090014 2017110010 2017110012 2017110013 2017110015 2017110016 2017110017 2017110019 2017110026 2017110027 2017110028 2018100043 2019080030 2019080051 2019080052 2019100001  2019100002 2019100003 2019100017 2019100018 2019100019 2019100020 2020030021 2020040001 2020040002 2020040003 2020040004 2020070021 2020070022 2020070023 2020070024 2020070025 2020120001 2021010002 2021010003 2021010004 2021030041 2021030042 2021030043 2021030044 2021030045 2021040021 2021040022
Recalling firm:
CooperSurgical, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled September 29, 2021

Hemodialysis Delivery System, Software Version 2.x.

If the operator initiates therapy with a saved prescription profile and makes a change to the prescription after a disposable filter change using the Same Patient button, the system may suggest values from the original prescription profile, rather than the current prescription.

ALL 50 STATES
Full report

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

Recall #:
88695
Lot/product code:
Software Version 2.x.;   Product Code: 955626, UDI: 0085412639499 (Lot/Serial #107208, 107209, 107210, 107211, 107378, 107379, 107380, 107381, 107382, 107383, 107384, 107385, 107386, 107387, 107483, 107484, 107485, 107486, 107487, 107488, 107489, 107490, 107491, 107492, 107493, 107494, 107495, 107496, 107497, 107498, 107499, 107500, 107501, 107502, 107503, 107504, 107505, 107506, 107507, 107508, 107509, 107510, 107511, 107512, 107818, 107819, 107820, 107821, 107822, 107823, 107824, 107825, 107826, 107827, 107878, 107879, 107880, 107881, 107882, 107883, 107884, 107885, 107886, 107887, 108193, 108194, 108195, 108196, 108197, 108198, 108199, 108200, 108201, 108202, 108203, 108204, 108205, 108206, 108207, 108208, 108209, 108210, 108211, 108212, 108303, 108304, 108305, 108306, 108307, 108308, 108309, 108310, 108311, 108312, 108453, 108454, 108455, 108456, 108457, 108458, 108459, 108460, 108461, 108462, 108503, 108504, 108505, 108506, 108507, 108508, 108509, 108510, 108511, 108512, 108777, 108778, 108779, 108780, 108781, 108782, 108783, 108784, 108785, 108786, 108842, 108843, 108844, 108846, 108847, 108848, 108849, 108850, 108851, 100121, 103416, 103417, 103418, 103419, 103420, 103421, 103422, 103423, 103424, 103425, 108845, 108934, 108935, 108936, 108938, 108940, 108942, 108947, 108951, 108952, 108954, 108956, 108958, 109081, 109082, 109083, 109084, 109085, 109086, 109087, 109088, 109089, 109090, 109091, 109092, 109093, 109094, 109095, 109096, 109097, 109098, 109099, 109100, 109171, 109172, 109175, 109176, 109178, 109179, 109180, 109181, 109182, 109183, 109186, 109189, 109190, 109324, 109325, 109326, 109327, 109328, 109329, 109330, 109331, 109332, 109333, 109334, 109335, 109336, 109337, 109338, 109339, 109340, 109341, 109342, 109343, 109344, 109345, 109346, 109347, 109348, 109349, 109350, 109551, 109552, 109553, 109554, 109555, 109556, 109557, 109558, 109559, 109560, 109561, 109562, 109563, 109564, 109565, 109566, 109567, 109568, 109569, 109570, 109571, 109572, 109573, 109574, 109575, 109576, 109577, 109578, 109579, 109580, 109740, 109741, 109742, 109743, 109744, 109745, 109746, 109747, 109748, 109749, 109750, 109751, 109752, 109753, 109754, 109755, 109756, 109757, 109758, 109759, 109760, 109761, 109762, 109763, 109764, 109765, 109766, 109767, 109768, 109769, 109810, 109811, 109812, 109813, 109814, 109815, 109816, 109817, 109818, 109819, 109820, 109821, 109822, 109823, 109824, 109825, 109826, HVER5, 101132, 101209, 101218, 101219, 101220, 101221, 101222, 101223, 101224, 101225, 101226, 101227, 101228, 101279, 101280, 101281, 101282, 101283, 101284, 101285, 101286, 101287, 101288, 101289, 101290, 101291, 101292, 101293, 101321, 101322, 101323, 101324, 101325, 101326, 101327, 101328, 101329, 101330, 101331, 101342, 101343, 101344, 101345, 101346, 101347, 101348, 101349, 101350, 101351, 101352, 101353, 101354, 101355, 101356, 101387, 101388, 101389, 101390, 101391, 101392, 101393, 101394, 101395, 101396, 101397, 101398, 101419, 101420, 101421, 101422, 101423, 101424, 101425, 101426, 101427, 101428, 101448, 101449, 101450, 101451, 101452, 101453, 101454, 101455, 101456, 101457, 101608, 101609, 101610, 101611, 101612, 101613, 101614, 101615, 101616, 101617, 101688, 101689, 101690, 101691, 101692, 101693, 101694, 101695, 101696, 101697, 101749, 101750, 101751, 101752, 101753, 101754, 101755, 101756, 101757, 101758, 101789, 101790, 101791, 101792, 101793, 101794, 101795, 101796, 101798, 102140, 102141, 102142, 102143, 102144, 102145, 102146, 102147, 102148, 102149, 102150, 102151, 102152, 102153, 102154, 102155, 102156, 102157, 102158, 102159, 102306, 102307, 102308, 102309, 102310, 102311, 102312, 102313, 102314, 102315, 102316, 102317, 102318, 102319, 102320, 102321, 102322, 102323, 102324, 102325, 102326, 102327, 102328, 102329, 102330, 102331, 102332, 102333, 102334, 102335, 102336, 102352, 102353, 102354, 102355, 102356, 102358, 102359, 102360, 102361, 102362, 102363, 102364, 102365, 102366, 102397, 102398, 102399, 102400, 102401.102402, 102404, 102405, 102406, 102407, 102408, 102409, 102410, 102411, 102412, 102413, 102414, 102415, 102416, 102417, 102418, 102419, 102420, 102421, 102422, 102423, 102424, 102425, 102426, 102457, 102458, 102459, 102460, 102461, 102462, 102463, 102464, 102465, 102466, 102467, 102468, 102469, 102470, 102471, 102487, 102488, 102489, 102490, 102491, 102492, 102493, 102494, 102495, 102496, 102497, 102498, 102499, 102500, 102501, 102876, 102877, 102878, 102879, 102880, 102881, 102882, 102883, 102884, 102885, 102886, 102887, 102888, 102889, 102890, 102891, 102892, 102893, 102894, 102895, 102896, 102897, 102898, 102899, 102900, 102921, 102922, 102923, 102924, 102925, 102926, 102927, 102928, 102929, 102930, 103186, 103187, 103188, 103189, 103190, 103191, 103192, 103193, 103194, 103195, 103196, 103197, 103198, 103199, 103200, 103201, 103202, 103203, 103204, 103205, 103206, 103207, 103208, 103209, 103210, 103211, 103212, 103213, 103214, 103215, 103216, 103217, 103218, 103219, 103220, 103221, 103… (truncated, 34214 characters total — see the official FDA record for the full value)
Recalling firm:
Baxter Healthcare Corporation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled September 29, 2021

LEEP PRECISION Generator 220V Cooper Surgical Part Number: LP-20-220

Coagulate function may not operate with the use of the Hand Switch, failure of the device to coagulate tissue may lead to a prolonged procedure requiring medical intervention to control any intraoperative bleeding and complete the case.

ALL 50 STATES
Full report

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

Recall #:
88648
Lot/product code:
Serial Numbers: 2018100001 2018100002 2018100003
Recalling firm:
CooperSurgical, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled September 29, 2021

LEEP PRECISION Integrated System, 220V CooperSurgical part numbers: LP-10-220

Coagulate function may not operate with the use of the Hand Switch, failure of the device to coagulate tissue may lead to a prolonged procedure requiring medical intervention to control any intraoperative bleeding and complete the case.

ALL 50 STATES
Full report

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

Recall #:
88648
Lot/product code:
Serial Numbers: 2017040001 2017040002 2017040003 2017040004 2017040005 2018030001 2018030002 2018030003 2018030004 2018100004 2018100005 2018100006 2018120001 2018120002 2018120003 2019010001 2019010002 2019010003 2019010004 2019010005 2019030001 2019030002 2019030003 2019030004 2019070001 2019070002 2019070003 2019070004 2019070005 2019070006 2019100001 2019100004 2019100005 2019120001 2019120002 2019120003 2019120004 2019120005 2019120006 2020030001 2020030002 2020030003 2020030004 2020030005 2020060001 2020060002 2020060003 2020060004 2020060005 2020060006 2020080001 2020080002 2020080003 2020080004 2020080005 2020080006 2020110001 2020110002 2020110003 2020110004 2020110005 2020110006 2020120001 2020120002 2020120003 2020120004 2020120005 2020120006 2021010001 2021010002 2021010003 2021010004 2021010005
Recalling firm:
CooperSurgical, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled September 29, 2021

Quantum 2000 Electrosurgical Generators Cooper Surgical Part Number: 909075

Coagulate function may not operate with the use of the Hand Switch, failure of the device to coagulate tissue may lead to a prolonged procedure requiring medical intervention to control any intraoperative bleeding and complete the case.

ALL 50 STATES
Full report

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

Recall #:
88648
Lot/product code:
Serial Numbers: 0112010 0209001 0214002 0309031 0313007BFIX 0411002 0609010FIX 0710001 0711008 0713011C 0809009 0813032CFIX 091402 1013009C 1013015C 1109017 1214005 2015090019 2015110003 2016030001 2016040012 2016060016 2016090003 2016110002 2017010005 2017060010 2017080010 QTMAA-4-095 QTM-AB-10-149 QTM-M-4-102FIX W110954 W351106 W60413 0114011 0212004 0214007 0312021 0313010B 0413003B 0612001B 0710003 0711008FIX 0713018C 0811017 0813033C 1011010 1013010C 1014004 1111002 2015040009 2015090021 2015110004 2016030002 2016040015 2016060020 2016090004 2016110003 2017020004 2017060013 AFZFIX QTMAA4101 QTM-AB-12-164 QTMY-11-0201 W204996 W381180 W605041 0114013 0212008 0214008 0312024 0313011B 0511002 0612003B 0710008 0711009 0714007 0811021 0813034C 1011010FIX 1013011C 1109008 1213005C 2015060003 2015100004 2015110009 2016040001 2016040018 2016070003 2016090007 2016110004 2017030002 2017080002 ATM-AA-4-106 QTMAA-4-102 QTM-AB-12-165 QTMY-12-0208 W2A1022 W381192 W708311FIX 0115006 0212010 0215005 0312033 0409005 0511003 0612010B 0710008FIX 0712009B 0809004 0811021FIX 0814011FIX 1012006B 1013012C 1109014 1213006C 2015090012 2015100006FIX 2015110010 2016040002 2016060012 2016070007 2016090014 2016120002 2017030005 2017080003 GHILL QTMAA6116 QTMAB3067 QTMY70139 W2B1036 W604009  0115007 0214001 0215007 0313001B 0409006 0511003FIX 0612016B 0711006 0713001C 0809007 0813029C 0814012 1013006C 1013014C 1109015 1214003 2015090015 2015110001 2016020006 2016040007 2016060013 2016080002 2016110001 2017010002 2017030009 2017080006 IUY80207 QTMAA-6-116 QTM-AB-9135 W107893 W2C1054 W604013
Recalling firm:
CooperSurgical, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled September 29, 2021

Quantum 2000 Electrosurgical Generators Cooper Surgical Part Number: 909075-05W

Xxx

ALL 50 STATES
Full report

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

Recall #:
88648
Lot/product code:
Serial Numbers:  0111001 0111003 0111004 0111005 0111006 0112001 0112002 0112003 0113001B 0113002B 0113003B 0113004B 0113005B 0113006B 0113007B 0113008B 0113010B 0114001 0114002 0114003 0114004 0114005 0114006 0114007 0114008 0114009 0114010 0209015 0215001 0215002 0215003 0215004 0215005 0215006 0215007 0215008 0215009 0215010 0215011 0312001 0312002 0312009 0312009FIX 0312010 0312028 0413001B 0414001 0414003 0414004 0414008 0414014 0414018 0512001B 0512002B 0513001B 0513002B 0513003B 0514005 0612023B 0612024B 0612025B 0612026B 0612027B 0612028B 0712001B 0712002B 0712003B 0712004B 0712005B 0712006B 0713001C 0713002C 0713003C 0713004C 0713005C 0713006C 0809001SYC 0813020C 0813021C 0813022C 0813023C 0813024C 0813025C 0814010 1012001B 1012002B 1012003B 1012004B 1012005B 1012006B 1012007B 1012008B 1012009B 1012010B 1109018 1109019 1113001C 1113002C 1113003C 1113004C 1113005C 1113006C 1113007C 1113008C 1113009C 1113010C 1213001 1213002 1213003 1214007 2015040001 2015040002 2015040003 2015040004 2015040005 2015050001 2015050002 2015060001 2015060002 2015060003 2015060004 2015060005 2015070004 2015090002 2015090003 2016050001 2016050005 2016070001 2016070002 2016070003 2016070004 2016070005 2016100001 2016100002 2016100003 2016100004 2016100005 2016100006 2016120002 2016120003 2016120004 2016120005 2016120006 2016120007 2016120008 2017060003 2017060005 QTM-AB-1-002 QTMAB-12-175
Recalling firm:
CooperSurgical, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled September 29, 2021

ARCHITECT c4000 REF 02P24-01/2P24, 1P86, 1R24, and 1R25; ARCHITECT c8000 REF 01G06-11/1G06; ARCHITECT c16000 REF 03L77-01/3L77;

Twelve software-related issues affecting software version 9.41 and earlier were identified. The issues include bypassing error codes, incorrect calibration, loss of module communication leading to overfilling wash buffer containers, missing QC flags, signal spikes, abnormal optics reads, and incorrect sample aspiration. The issues may lead to inaccurate results with an unknown bias direction and magnitude for assays measuring cardiac, metabolic (including diabetes), toxicology, prenatal, therapeutic drug monitoring, infectious disease, oncology, hepatic, pancreatic, hematological, endocrinologic, inflammatory analytes.

Full report

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

Recall #:
88880
Lot/product code:
Product Description/List Number ARCHITECT c4000 Module List Number: 2P24 UDI: (01)00380740003746(21)c4123456(240)02P2401 Serial Numbers: C400000 C400010 C400011 C400012 C400013 c400014 c400015 C400016 C400017 C400018 C400019 C400020 C400023 C400024 C400025 C400026 C400027 C400030 C400031 C400032 C400034 C400035 C400036 C400038 C400039 C400040 C400041 C400042 C400043 C400045 C400046 C400047 C400049 C400050 C400051 C400053 C400054 C400055 C400056 C400057 C400058 C400060 C400061 C400062 C400063 C400064 C400065 c400066 C400067 C400068 C400069 C400070 C400071 C400072 C400073 C400074 C400075 C400077 C400078 C400079 C400080 C400081 C400083 C400084 C400085 C400086 C400087 C400089 C400090 C400091 C400092 C400093 C400095 C400096 C400098 C400099 C400100 C400101 C400102 C400104 C400105 C400106 C400107 C400108 C400109 C400112 C400114 C400115 C400116 C400117 C400118 C400119 C400120 C400121 C400122 C400123 C400124 C400125 C400127 C400129 C400132 C400133 C400134 C400135 C400136 C400137 c400139 C400140 C400141 C400142 C400143 C400144 C400145 C400146 C400147 C400148 C400149 C400150 C400151 C400152 C400153 C400154 C400155 C400156 C400157 C400158 C400159 C400160 C400161 C400162 C400163 C400164 C400165 C400166 C400167 C400168 C400169 C400170 C400171 C400172 C400173 C400174 C400175 C400176 C400177 C400178 C400179 C400182 C400183 C400184 C400185 C400186 C400187 C400188 C400189 C400190 C400191 C400192 C400195 C400196 C400197 C400199 C400200 C400201 C400202 C400203 C400204 C400205 C400206 C400207 C400209 C400210 C400211 C400212 C400213 C400214 C400215 C400217 C400218 C400220 C400222 C400223 C400224 C400227 c400228 C400229 C400230 C400231 C400232 C400234 C400235 C400236 C400237 C400238 C400239 C400240 C400241 C400242 C400243 C400244 C400245 C400246 C400247 C400248 C400250 C400251 C400252 C400253 C400254 C400256 C400258 C400259 C400260 C400261 C400262 C400263 C400264 C400266 C400268 C400269 C400270 C400271 C400273 C400274 C400275 C400276 C400277 C400278 c400279 C400280 C400281 C400282 C400283 C400284 C400285 C400287 C400288 C400289 C400290 C400291 C400292 C400293 C400294 C400295 C400296 C400297 C400298 C400299 C400300 C400301 C400302 C400303 C400304 C400305 C400306 C400307 C400309 C400310 C400312 C400313 C400315 C400316 C400317 C400318 C400319 C400320 C400321 C400322 C400324 C400325 C400326 C400327 C400328 C400329 C400331 C400332 C400333 C400334 C400335 C400337 C400338 C400340 C400341 C400342 C400344 C400345 C400347 C400348 C400349 C400350 C400351 C400352 C400354 C400355 C400356 C400357 C400358 C400359 C400362 C400363 C400364 C400365 C400366 C400367 C400368 C400369 C400370 C400371 C400373 C400374 C400375 C400376 C400377 C400378 C400379 C400380 C400381 C400382 C400383 C400384 C400385 C400386 C400387 C400388 C400389 C400390 C400391 C400392 C400393 C400394 C400395 C400397 C400398 C400399 C400400 C400402 C400403 C400404 C400405 C400406 C400407 C400408 C400409 C400410 C400411 C400412 C400413 C400414 C400415 C400416 c400417 C400418 C400419 C400420 C400422 C400423 C400424 C400425 C400426 C400427 C400428 C400429 C400430 C400431 C400432 C400433 C400434 C400435 C400436 C400437 C400439 C400440 c400442 C400443 C400444 C400445 C400446 C400447 C400448 C400449 C400450 C400451 C400453 C400454 C400455 C400456 C400457 C400459 C400460 C400461 C400463 C400464 C400465 C400466 C400467 C400468 C400469 C400470 C400471 C400472 C400473 C400474 C400475 C400476 C400477 C400478 C400479 C400480 C400481 C400482 C400483 C400484 C400485 C400486 C400487 C400488 C400489 c400490 C400491 C400492 C400493 c400494 C400495 C400496 C400497 C400498 C400499 C400500 C400501 C400502 C400503 C400504 C400505 C400508 C400509 C400510 C400511 C400512 C400513 C400514 C400515 C400516 C400518 c400519 C400520 C400521 C400522 C400523 C400524 C400525 C400526 C400527 C400528 C400529 C400530 C400531 C400532 C400533 C400534 C400535 C400536 C400537 C400538 C400539 C400540 c400541 C400542 C400543 C400544 C400545 C400546 C400547 C400548 C400549 c400550 C400551 C400552 C400554 c400555 C400556 C400557 C400558 C400559 C400560 C400561 C400562 C400563 C400564 C400565 C400566 C400567 C400568 C400569 C400570 C400571 C400572 C400573 C400574 C400575 C400576 C400577 C400578 C400579 C400580 C400581 C400582 C400583 C400584 C400585 C400586 C400587 C400588 C400589 C400590 C400591 C400593 C400594 C400595 C400596 C400597 C400598 C400599 C400600 C400601 C400602 C400603 C400604 C400605 C400606 C400607 C400608 c400609 C400610 C400611 C400612 C400614 C400616 C400617 C400618 C400619 C400620 C400621 C400622 C400623 C400624 C400625 C400626 C400627 C400629 C400630 C400631 C400632 C400633 C400634 C400635 C400636 C400637 C400638 C400639 C400640 C400641 C400642 C400643 C400645 C400646 C400647 C400648 C400649 C400650 C400651 C400652 C400653 C400654 C400655 C400656 C400657 C400658 C400659 C400660 C400661 C400662 C400663 c400664 C400665 C400666 C400667 C400668 C400669 C400670 c400671 c400672 C400673 C400675 C400676 C400677 C400678 C400679 C400680 C400681 C400682 C400683 C400684 C400685 C400686 C400687 C400688 C400689 C400690… (truncated, 99077 characters total — see the official FDA record for the full value)
Recalling firm:
Abbott Laboratories
View official FDA record (opens in a new tab)