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 deaths or serious injuries are reported, 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

22026–22050 of 25981

HighFDA (Drugs)·D-0730-2022·2022-04-06
Injectable testosterone-anastrozole mixture recalled for sterility assurance failure
Drug Depot (APS Pharmacy) is recalling testosterone cypionate/anastrozole injectable oil due to lack of sterility assurance. The recall affects 846 vials distributed nationwide.
Product
TESTOSTERONE CYPIONATE/ANASTROZOLE *GS* OIL 200MG/1MG/ML Injectable, Packaged in a multi dose 10ML vial, as a) 4 ML Formula ID 115387; b) (RM) 10 ML Formula ID 115125; APS Pharmacy
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0916-2022·2022-04-06
Carbquik Complete Biscuit Mix Recalled for Undeclared Milk Allergen
Tova Industries Inc is recalling Carbquik Complete Biscuit and Baking Mix due to undeclared milk allergen. The recall affects 224 cases distributed through an Amazon distribution center in New Mexico.
Product
Carbquik Complete Biscuit and Baking Mix, Net Wt. 3lb *Contained 1 free sample of Cinnamon Spice Mug Cake
Category
Food
Distribution
1 state
HighFDA (Devices)·Z-0835-2022·2022-04-06
Tissue oximeter module may provide inaccurately low oxygen readings
Edwards Lifesciences is recalling 8,389 FORE-SIGHT ELITE Tissue Oximeter modules that may display inaccurately low oxygen saturation values when used in certain body locations, potentially leading to inappropriate treatment decisions.
Product
FORE-SIGHT ELITE Tissue Oximeter module, REF: HEMFSM10
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0736-2022·2022-04-06
Glycopyrrolate Tablets Recalled Due to Glass Pieces in Sealed Bottles
Aurolife Pharma is recalling Glycopyrrolate Tablets after glass fragments were discovered in a sealed bottle from packaging equipment. Approximately 4,080 bottles were distributed nationwide and in Puerto Rico.
Product
GLYCOPYRROLATE — GLYCOPYRROLATE (GLYCOPYRROLATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0842-2022·2022-04-06
Ceramic Hip Femoral Head Component May Not Match Package Label
Howmedica Osteonics is recalling certain Biolox delta Ceramic V40 Femoral Head components because the actual size and offset may not match the package label. Patients with these implants should contact their surgeon.
Product
Biolox delta Ceramic V40 Femoral Head 32/ -4.0mm Catalog Number: 6570-0-032
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0917-2022·2022-04-06
Tam's Homemade Biscuits recalled for missing allergen and ingredient labels
Tam's Homemade Biscuits (Batch No. 015-022) are recalled due to missing allergen statement and ingredient list. Consumers with food allergies cannot identify potential allergens in the product.
Product
Tam's Homemade Biscuits 8 count packaged in 9 inch round aluminum cake pan 10 pans per case
Category
Food
Distribution
0 states
HighFDA (Drugs)·D-0732-2022·2022-04-06
Testosterone Cypionate Injectable Recalled Due to Lack of Sterility Assurance
Drug Depot, Inc. is recalling 620 vials of Testosterone Cypionate/DHEA injectables due to lack of sterility assurance in manufacturing. The product was distributed nationwide.
Product
TESTOSTERONE CYPIONATE/ DHEA *GS* 200/10MG/ML Injectable, Packaged in a multi dose 10ML vial, as a) 5 ML Formula ID 115678; b) 10 ML Formula ID 115498, APS Pharmacy
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0834-2022·2022-04-06
FORE-SIGHT ELITE Tissue Oximeter: Inaccurate Oxygen Saturation Readings
Edwards Lifesciences FORE-SIGHT ELITE Absolute Tissue Oximeter (Model 01-06-3000) is recalled because StO2 (tissue oxygen saturation) values may read inaccurately low when used with the large sensor on arms or legs, potentially leading to inappropriate treatment.
Product
FORE-SIGHT ELITE Absolute Tissue Oximeter, REF: 01-06-3000, Contents: Monitor 1 EA., Accessory Kit 1 EA.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0853-2022·2022-04-06
Surgical Drill System Instrument Pack Recalled Over Device Breakage Risk
Wright Medical is recalling 176 packs of the EasyFuse Dynamic Compression System Instrument Pack due to risk that the drill guide can jam and break during surgery.
Product
EasyFuse Dynamic Compression System Instrument Pack
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0841-2022·2022-04-06
Radiographic system software error may cause unintended tube stand movement
Siemens is recalling 70 Ysio radiographic systems due to a software error that may cause unintended tube stand movement and create collision risk.
Product
Ysiosystem with VC10 software version, Model Number 10281013. Radiographic system
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0728-2022·2022-04-06
FDA Recalls Gonadorelin Injectable Vials for Lack of Sterility Assurance
Drug Depot, Inc. is recalling Gonadorelin 0.2 mg/mL injectable vials distributed nationwide due to lack of sterility assurance. Approximately 6,017 vials are affected.
Product
GONADORELIN (5ML) 0.2 MG/ML INJECTABLE, Packaged in a multi dose 10ML vial, Formula ID132227, APS Pharmacy
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0960-2022·2022-04-06
Good & Gather Dried Strawberries Recalled for Undeclared Sulfites
Good & Gather Dried Sweetened Strawberries are being recalled due to undeclared sulfites. Consumers with sulfite sensitivity should not consume this product.
Product
Good & Gather Dried Sweetened Strawberries. Net Wt 4 oz (113g). UPC 085239-182840 No Sulfites Added. No Artificial Flavors. No Synthetic Colors. Distributed by Target Corporation, Minneapolis, MN 55403
Category
Food
Distribution
20 states
HighFDA (Devices)·Z-0847-2022·2022-04-06
BALLARD Multi-Access Port Catheter Recalled for Incorrect Expiration Date
Avanos Medical is recalling 2,520 BALLARD Multi-Access Port Catheters due to incorrect expiration dates on the packaging. No illnesses or injuries have been reported. Patients should verify the lot number and contact their healthcare provider.
Product
BALLARD* Multi-Access Port (MAP) Catheter, Double Swivel Y- Adult, 16 French; Sterile; Single Use
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0830-2022·2022-04-06
Siemens Magnesium Flex reagent cartridge recalled for imprecision and assay errors
Siemens recalls magnesium reagent cartridges due to imprecision and abnormal assay flags that may cause erroneous diagnostic results and require repeat patient testing.
Product
Siemens Dimension Vista Magnesium Flex reagent cartridge (MG) Material # 10445158, Catalog # K3057 used in the Dimension Vista System. The Dimension Vista Magnesium Flex Reagent (MG) method is an In vitro diagnostic test for the quantitative measurement of magnesium in human
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0733-2022·2022-04-06
Injectable Testosterone Recalled Due to Lack of Sterility Assurance
Drug Depot's testosterone injection product was recalled nationwide for lack of sterility assurance. Affected consumers should discontinue use and consult their healthcare provider.
Product
TESTOSTERONE CYPIONATE/PROPIONATE *SES* Oil (10 ML) 160MG/20MG/ML Injectable, Packaged in a multi dose 10ml vial, Formula ID 115498, APS Pharmacy
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0729-2022·2022-04-06
Gonadorelin injectable recalled for lack of sterility assurance
Drug Depot recalls 1,843 vials of Gonadorelin injectable nationwide due to lack of sterility assurance. Patients should consult their healthcare provider regarding previously dispensed doses.
Product
(CA) GONADORELIN (4ML) 0.2 MG/ML INJECTABLE, Packaged in a multi dose 10ML vial, Formula ID136345, APS Pharmacy
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0826-2022·2022-04-06
Retinal Analysis Software with Potentially Unapproved AI Features Recalled
Diagnos Inc is recalling CARA retinal analysis software version 4.7.2 because some AI-based features may lack appropriate FDA market approval. Users are advised to revert to a prior software version.
Product
CARA (Computer Assisted Retinal Analysis), Product ID: +B543CARA0/$$+7V4.7.2/16D202111179
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-0854-2022·2022-04-06
Illumina NextSeq 550Dx DNA Analyzer Recalled for Short Circuit Risk
Illumina is recalling 674 NextSeq 550Dx DNA sequence analyzers worldwide. A short circuit may occur after reconnecting circuit components, causing the device to become inoperable.
Product
Illumina NextSeq 550Dx, REF: 20005715, CE, IVD
Category
Medical Device
Distribution
31 states
HighNHTSA·22V226000·2022-04-06
2022 Volkswagen Tiguan rear spoiler risks detaching from vehicle
2022 Volkswagen Tiguan vehicles are recalled due to insufficient attachment of the rear hatch spoiler. The spoiler may separate from the vehicle, creating a road hazard and increasing crash risk.
Product
VOLKSWAGEN — 2022 VOLKSWAGEN TIGUAN
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0735-2022·2022-04-06
Testosterone Cypionate Injectable Recalled for Lack of Sterility Assurance
Drug Depot recalled 17 vials of Testosterone Cypionate Injectable due to lack of sterility assurance in manufacturing. The recalled product was distributed nationwide and should not be used.
Product
TESTOSTERONE CYPIONATE *GS* (2 mL) 80 MG/ML Injectable, Packaged in a multi dose 10ML vial, Formula ID 127492, APS Pharmacy
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0843-2022·2022-04-06
Hip prosthetic femoral head component size and offset labeling mismatch
Howmedica Osteonics is recalling 40 units of Biolox delta Ceramic V40 Femoral Head components where the size and/or offset may not match package labeling.
Product
Biolox delta Ceramic V40 Femoral Head 32/ +4.0mm Catalog Number: 6570-0-232
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0832-2022·2022-04-06
Ambulatory infusion pumps recalled due to erroneous software installation
InfuTronix is recalling Nimbus PainPro ambulatory infusion pumps after an unreleased software version was installed in error. The defective units may impact patient safety.
Product
Nimbus PainPro Ambulatory Infusion Pumps with software version v4, Model Number IT1072, sold as kit IT1075-DUKE-HSP, IT1076-DUKE-HSP and IT1077-DUKE-HSP
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0849-2022·2022-04-06
Radiation therapy planning software: incorrect dose density calculation
RayStation/RayPlan radiation therapy software (versions 4–11A) may incorrectly calculate radiation dose density in treatment planning. The error affects dose calculations in regions partially covered by certain structures.
Product
RayStation/RayPlan versions 4 - 11A, including service packs. Build Stations: 4.0.0.14, 4.0.3.4, 4.3.0.14, 4.5.1.14, 4.7.2.5, 4.7.3.13, 4.7.4.4, 4.7.5.4, 4.7.6.7, 4.9.0.42, 5.0.1.11, 5.0.2.35, 5.0.3.17, 6.0.0.24, 6.1.1.2, 6.2.0.7, 6.3.0.6, 7.0.0.19, 8.0.0.61, 8.0.1.10, 8.1.0.47,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0848-2022·2022-04-06
Radiation therapy planning software subject to jaw positioning errors during optimization
RayStation radiation therapy planning software (versions 6-11A) may unexpectedly change jaw positions during optimization after dose or target modifications. Users should verify treatment plans carefully before delivery.
Product
TomoHelical and TomoDirect plans in RayStation 6, 7, 8A, 8B, 9A, 9B, 10A, 10B and 11A. Build Numbers: 6.1.1.2, 6.2.0.7, 6.3.0.6, 7.0.0.19, 8.0.0.61, 8.0.1.10, 8.1.0.47, 8.1.1.8, 8.1.2.5, 9.0.0.113, 9.1.0.933, 9.2.0.483, 10.0.0.1154, 10.0.1.52, 10.1.0.613, 11.0.0.951 or 11.0.1.2
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0734-2022·2022-04-06
Testosterone Cypionate Injectable Vials Recalled for Lack of Sterility Assurance
Drug Depot, Inc. is recalling 24 vials of Testosterone Cypionate 200 MG/ML Injectable nationwide due to lack of sterility assurance. The product was distributed throughout the USA and Puerto Rico.
Product
TESTOSTERONE CYPIONATE *GS* Oil 200 MG/ML Injectable, Packaged in a multi dose 10ML vial, Formula ID 76681, APS Pharmacy
Category
Drug
Distribution
Distributed nationwide

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22026–22050 of 25981