Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

16226–16250 of 40112

HighFDA (Devices)·Z-3026-2020·2020-10-07
Zeus ELISA Parvovirus B19 IgM Test System Recalled for False Positives
Zeus Scientific is recalling 74 units of the ZEUS ELISA Parvovirus B19 IgM Test System due to false positive results identified during an FDA inspection.
Product
ZEUS ELISA Parvovirus B19 IgM Test System, UDI 00845533001755 - Product Usage: intended for the qualitative detection of IgM class antibodies to human Parvovirus B19 in human serum including women of childbearing age where there is a suspicion of exposure to human Parvovirus…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3042-2020·2020-10-07
Ameditech Recalls ProScreen Drugs of Abuse Tests Due to Performance Failures
Ameditech is recalling ProScreen Drugs of Abuse Tests because immunoassay enzymes failed performance standards, causing inconsistent detection of compounds.
Product
ProScreen" Drugs of Abuse Test (AMT Item/ AMT Description): PSD-6MB/ "ProScreen" Drugs of Abuse Test (MET1000/OPI2000)+AMP+BZO+COC+THC", PSD-6MTDBO-300 /"ProScreen" Drugs of Abuse Test (COC/THC)+BZO+MTD+OPI300+OXY", PSCUP-5M-W/ ProScreen" Drugs of Abuse Cup…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0025-2021·2020-10-07
Riverpoint Medical Recalls Non-Sterile Velosorb Surgical Sutures
Riverpoint Medical is recalling 1,267 units of Velosorb Fast Braided Absorbable Sutures because they are non-sterile. The defect could compromise the sterile field and increase the risk of surgical site infections.
Product
Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 4/0 Undyed 18" P-12 Cutting, Product Number: SV496G, UDI: 20884521149691 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0043-2021·2020-10-07
Riverpoint Recalls Non-Sterile Velosorb Surgical Sutures
Riverpoint Medical is recalling 1,244 units of Velosorb Fast Braided Absorbable Sutures because they are non-sterile, posing a risk of surgical site infection.
Product
Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 4/0 Undyed 30" KV-15 TaperCutting CV2279, UDI: 20884521151632 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not for use…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0040-2021·2020-10-07
Riverpoint Recalls Non-Sterile Velosorb Surgical Sutures
Riverpoint Medical is recalling 1,242 units of Velosorb Fast Braided Absorbable Sutures because they are non-sterile, posing a risk of surgical site infection.
Product
Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 4/0 Undyed 30" P-12 Cutting SV426, UDI: 20884521151731 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not for use in…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0022-2021·2020-10-07
Riverpoint Recalls Non-Sterile Velosorb Fast Braided Absorbable Sutures
Riverpoint Medical is recalling 1,270 units of Velosorb Fast Braided Absorbable Sutures because they are non-sterile, posing a risk of surgical site infection.
Product
Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 6/0 VL 18" P-10, Product Number: SV32, UDI: 20884521153117 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not for use in…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3036-2020·2020-10-07
Ameditech Recalls ImmuTest Drugs of Abuse Cups for Performance Failures
Ameditech is recalling ImmuTest Drugs of Abuse Cups because they failed to consistently detect all compounds at labeled levels.
Product
ImmuTest Drugs of Abuse Cup (AMT Item Number/ AMT Description): IMCA-5AB-W / "ImmuTest Drugs of Abuse Cup AMP1000+BZO300+COC300+OPI2000+THC50 With Cr, Ni, pH, Bl, S.G.", IMC-8BBCE/ "ImmuTest Drugs of Abuse Cup 8 Drug Detection…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3022-2020·2020-10-07
Encore Medical Recalls Humeral Socket Inserts Due to Size Mismatch
Encore Medical is recalling 37 humeral socket inserts because the size etched on the product may differ from the size on the patient sticker label.
Product
RSP Standard HUMERAL SOCKET INSERT, 40 MM plus 4MM, HXe-Plus, Part No. 509-00-440
Category
Medical Device
Distribution
12 states
HighFDA (Devices)·Z-3049-2020·2020-10-07
Ameditech Recalls First Check 4 Panel Drug Cups Due to Performance Failures
Ameditech Inc is recalling 537,120 units of First Check 4 Panel Drug Cups because they may fail to consistently detect all compounds at labeled levels.
Product
First Check 4 Panel Drug Cup: COC/MET1000/OPI2000/THC): (THC/COC); AMT Item Number 990100B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3017-2020·2020-10-07
Olympus BF-Q180 Bronchovideoscope Recalled for Infection Risk and Regulatory Issues
Olympus is recalling BF-Q180 bronchovideoscopes because they lack 510(k) clearance and are associated with a higher rate of patient infections.
Product
Olympus Medical Systems Corporation (OMSC) Evis Exera II Bronchovideoscope Olympus BF Type Q180 (BF-Q180) All serial numbers - Product Usage: designed to be used with an Olympus video system center, light source, documentation equipment, monitor, EndoTherapy accessories (such as…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3037-2020·2020-10-07
Ameditech MicroScreen Immunoassay Recalled for Inconsistent Detection Performance
Ameditech Inc is recalling 23,000 MicroScreen immunoassay units because they failed to consistently detect compounds at labeled levels.
Product
MicroScreen (AMT Item Number/ AMT Description): MSCA-6MBAU/ "MicroScreen AMP300/BZO200/COC300/MET300/OPI300/ THC50 with Cr, Ni, pH, Bl, S.G. "
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3024-2020·2020-10-07
Office Depot Recalls JINYINSHAN KN95 Masks Due to Filtration Failure
Office Depot is recalling 25,360 JINYINSHAN KN95 masks because test results showed they failed to filter more than 95% of particulates.
Product
JINYINSHAN, KN95 PROTECTIVE MASK P1, 20 pieces
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3021-2020·2020-10-07
Encore Medical Recalls Mislabeled Humeral Socket Inserts
Encore Medical is recalling 15 units of RSP Standard Humeral Socket Inserts due to size labeling discrepancies that could lead to incorrect implantation.
Product
RSP Standard HUMERAL SOCKET INSERT, 44MM, HXe-Plus, Part No. 509-00-044
Category
Medical Device
Distribution
12 states
HighFDA (Devices)·Z-0005-2021·2020-10-07
Endo GIA Auto Suture Universal Loading Unit Recall for Staple Formation Defect
FDA is recalling Endo GIA Auto Suture Universal Loading Units because staples may not form properly, potentially preventing adequate hemostasis during surgery.
Product
Endo GIA Auto Suture Universal Loading Unit 45 mm - 2.5mm, Item Code 030454 - Product Usage: The Endo GIA universal staplers have applications in abdominal, gynecologic, pediatric and thoracic surgery for resection, transection and creation of anastomosis.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3038-2020·2020-10-07
Ameditech MicroTox Immunoassay Enzymes Recalled for Performance Failures
Ameditech Inc is recalling MicroTox immunoassay enzymes because they failed to consistently detect compounds at labeled levels.
Product
MicroTox (AMT Item Number/ AMT Description): MTPA-6MBAU / "MicroTox (AMP300/BZO200)+(COC300/THC50)+ (MET300/MOR300) With Cr, Ni, pH, Bl, S.G.", MTPA-6MBAU/ "MicroTox (AMP300/BZO200)+(COC300/THC50)+ (MET300/MOR300) With Cr, Ni, pH, Bl, S.G."
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3015-2020·2020-10-07
Stryker IsoAir 2.0 Support Surface Recalled for CPR Connector Defect
Stryker is recalling 110 IsoAir 2.0 support surfaces because a connector defect may delay CPR during cardiac arrest.
Product
Stryker IsoAir 2.0 support surface-provides pressure redistribution and is intended to assist in management of the microclimate of the patient skin, Model Number: 2941-001-100
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0014-2021·2020-10-07
Riverpoint Recalls Non-Sterile Velosorb Surgical Sutures
Riverpoint Medical is recalling non-sterile Velosorb sutures that could compromise the sterile field and increase the risk of surgical site infection.
Product
Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 4/0 Undyed 30" C-12 Cutting, Product Number: SV2294, UDI 20884521151403 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0036-2021·2020-10-07
Riverpoint Recalls Non-Sterile Velosorb Surgical Sutures
Riverpoint Medical is recalling 1,272 units of Velosorb Fast Braided Absorbable Sutures because they are non-sterile. This condition could compromise the sterile field and increase the risk of surgical site infection.
Product
Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 0 Undyed 36" GS-21 Taper CV946, UDI: 20884521151298 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not for use in…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0011-2021·2020-10-07
Riverpoint Medical Recalls Non-Sterile Velosorb Surgical Sutures
Riverpoint Medical is recalling non-sterile Velosorb sutures because their use could compromise the sterile field and increase the risk of surgical site infection.
Product
Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 3/0 Undyed 30" P-14 Cutting, Product Number: SV935, UDI: 20884521151755 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0021-2021·2020-10-07
Riverpoint Recalls Non-Sterile Velosorb Surgical Sutures
Riverpoint Medical is recalling 1,248 units of Velosorb Fast Braided Absorbable Sutures because they are non-sterile, posing a risk of surgical site infection.
Product
Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 3/0 Undyed 30" SC-1, Product Number: SV2239, UDI: 20884521151779 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not for…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0001-2021·2020-10-07
Endo GIA Stapler Loading Units Recalled for Staple Formation Defects
FDA recalls Endo GIA Auto Suture Loading Units because staples may not form properly, potentially preventing adequate hemostasis during surgery.
Product
Endo GIA Auto Suture Gray Universal Articulating Loading Unit 30 mm - 2.0 mm, Item Code 030450 - Product Usage: The Endo GIA universal staplers have applications in abdominal, gynecologic, pediatric and thoracic surgery for resection, transection and creation of anastomosis.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0013-2021·2020-10-07
Riverpoint Medical Recalls Non-Sterile Velosorb Surgical Sutures
Riverpoint Medical is recalling 3,109 units of non-sterile Velosorb sutures distributed nationwide. The defect poses a risk of surgical site infection.
Product
Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 0 Undyed 36" KV-34 TaperCutting, Product Number: CV919, UDI: 20884521151649 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3020-2020·2020-10-07
Exactech Recalls Equinoxe Reverse Shoulder Compression Screw Kits
Exactech is recalling Equinoxe Reverse Shoulder Compression Screw/Locking Cap Kits because they may contain screws of incorrect length.
Product
Equinoxe Reverse Shoulder Compression Screw/Locking Cap Kit 4.5 x 22 mm.
Category
Medical Device
Distribution
23 states
HighFDA (Devices)·Z-3046-2020·2020-10-07
Ameditech Recalls First Check 1 Panel Drug Cup Due to Performance Failures
Ameditech Inc is recalling First Check 1 Panel Drug Cup (THC) units because immunoassay enzymes failed performance tests, preventing consistent detection of compounds.
Product
First Check 1 Panel Drug Cup: (THC); AMT Item Number 990400B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0029-2021·2020-10-07
Riverpoint Medical Recalls Non-Sterile Velosorb Surgical Sutures
Riverpoint Medical is recalling 2,499 units of Velosorb Fast Braided Absorbable Sutures because they are non-sterile. The defect could compromise the sterile field and increase the risk of surgical site infection.
Product
Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 4/0 Undyed 18" P-12 Cut, Product Number: SV496, UDI: 20884521184258 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not…
Category
Medical Device
Distribution
Distributed nationwide

How to read this listing

Filters

16226–16250 of 40112