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

25751–25775 of 114516

SevereFDA (Devices)·Z-0929-2023·2023-02-08
SARS-CoV-2 Antigen Rapid Test Kits Recalled for Lack of FDA Authorization
Universal Meditech Inc. is recalling approximately 56,300 SARS-CoV-2 Antigen Rapid Test Kits distributed without FDA approval, clearance, or Emergency Use Authorization. Products were distributed nationwide in California and Texas.
Product
Products are labeled as: Skippack Medical Lab SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold) 20 TESTS/1 KIT Green and white box under the brand DiagnosUS, and, White box without brand name labeled as "SARS -COV-2 ANTIGEN DEVELOPMENT MADE IN USA ORAL SWAB…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0247-2023·2023-02-08
FDA Recalls First Aid Cream Packets Over Bacterial Contamination
The FDA is recalling Adventure First Aid 1.5 first aid kits due to bacterial contamination found in the included burn cream packets. The contamination was identified through FDA laboratory testing.
Product
Adventure First Aid 1.5, First Aid Kit, containing Easy Care first aid After Burn Cream 0.9 g packets, Product # 0120-0212
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0319-2023·2023-02-08
James Farm Frozen Red Raspberries Recalled for Hepatitis A Contamination
James Farm brand frozen red raspberries from Chile may be contaminated with Hepatitis A Virus. The product was distributed to food service facilities in the Northeast.
Product
James Farm brand Frozen Red Raspberries; 2-5lb Bags; NET WT 10 LB (4.5 kg); KEEP FROZEN; IQF; Individually Quick Frozen; FOR FOOD SERVICE SALE ONLY; Distributed by: RD/JET, LLC; 15-24 132nd Street, College Point, NY 11356; Country of Origin: CHILE.
Category
Food
Distribution
8 states
SevereFDA (Drugs)·D-0251-2023·2023-02-08
FDA Recalls Easy Care First Aid Kit for Bacterial Contamination
The FDA is recalling Easy Care First Aid Kits with contaminated After Burn Cream packets distributed nationwide and in Canada. Lab testing identified Bacillus lichenformis and Bacillus sonorensis contamination.
Product
Easy Care First Aid 25 Person 2009 ANSI, First Aid Kit, containing Easy Care first aid After Burn Cream 0.9 g packets, Product # 9999-2132
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1031-2023·2023-02-08
Procedural trays recalled for potential sterile packaging breach
Medline Industries recalls non-sterile procedural trays (LAPAROTOMY CDS) because sterile blades within the kits may puncture the outer foil packaging, compromising sterility.
Product
Non-sterile procedural trays labeled as LAPAROTOMY CDS, 2 per case
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0333-2023·2023-02-08
Ameripack Foods Chocolate Brownies Recalled for Undeclared Soy and Egg
Ameripack Foods LLC is recalling Chocolate Chunk Brownies (UPC 4122077413) due to undeclared soy and egg allergens. Consumers with allergies to these ingredients should not consume the product.
Product
Chocolate Chunk Brownie 13oz UPC 4122077413 packaged in a metal tray with a clear plastic nonflexible lid, 6 trays per case
Category
Food
Distribution
1 state
HighFDA (Food)·F-0332-2023·2023-02-08
Frozen Breakfast Burrito Recalled for Undeclared Milk Allergen
Alpha Plant-Based Burrito products contain undeclared milk that poses an allergen risk. THE MISO BROTHERS INC is recalling 31,092 units distributed throughout US retail locations.
Product
Alpha Plant-Based Burrito - Steakless Ranchero 5.5 oz UPC 855099007764 Frozen
Category
Food
Distribution
0 states
HighFDA (Devices)·Z-1040-2023·2023-02-08
Siemens Fluoroscopic X-ray Systems Risk of Boot Failure After Shutdown
Certain Siemens fluoroscopic X-ray systems may only boot into backup mode after an abrupt shutdown, preventing full operation. This could necessitate cancelling or switching to alternative treatment systems.
Product
System Material # Artis zee floor 10094135 Artis zee ceiling 10094137 Artis zee multi-purpose 10094139 Artis zee biplane 10094141 Artis zeego 10280959 Artis Q floor 10848280 Artis Q ceiling 10848281 Artis Q biplane 10848282 Artis Q.zeego 10848283 Artis Q.zen floor…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1046-2023·2023-02-08
Medline UNITE Foot & Ankle Screw Recalled for Intra-Operative Failure
Medline Industries is recalling 420 units of UNITE FOOT & ANKLE Screws nationwide due to observed intra-operative screw failure when used with specific drill bit sizes. The failure occurs due to excessive torque during surgical insertion.
Product
MEDLINE UNITE FOOT & ANKLE Screw, Polyaxial Locking, Mini T8 (2.0x8mm), REF MMSL2008
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1035-2023·2023-02-08
Non-sterile procedural knee trays recalled for potential packaging breach
Medline Industries recalls non-sterile Total Knee procedural trays because sterile blades inside can puncture the outer foil packaging. This could compromise sterile blade integrity.
Product
Non-sterile procedural trays labeled as TOTAL KNEE KIT, 1 per case
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0325-2023·2023-02-08
Frozen Breakfast Burritos Recalled for Undeclared Milk Allergen
The Miso Brothers is recalling Alpha Plant Based Breakfast Burritos because they contain undeclared milk. This poses a risk to consumers with milk allergies or sensitivities.
Product
Alpha Plant Based Breakfast Burrito - BAC'N SCRAMBLE 5.5 oz. UPC 855099007948 Frozen
Category
Food
Distribution
0 states
HighFDA (Food)·F-0329-2023·2023-02-08
Frozen breakfast burritos recalled for undeclared milk allergen
THE MISO BROTHERS INC is recalling Alpha Plant-Based Burrito - CHIK'N FAJTA frozen breakfast burritos because they contain undeclared milk that is not listed on the label. The product poses a risk to consumers with milk allergies.
Product
Alpha Plant-Based Burrito - CHIK'N FAJTA 5.5 oz UPC 855099007047 Frozen
Category
Food
Distribution
0 states
HighFDA (Devices)·Z-1025-2023·2023-02-08
Cardiopulmonary Bypass Oxygenator Recalled for Loose Temperature Monitoring Adapter
Medtronic Perfusion Systems is recalling 1,340 units of the Affinity Fusion Oxygenator due to reports that the Temperature Monitoring Adapter can come loose during or after use in cardiopulmonary bypass procedures.
Product
Affinity Fusion Oxygenator with Integrated Arterial Filter and Balance Biosurface, Custom Packs, REF CB811. Used in Cardiopulmonary bypass.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1034-2023·2023-02-08
Procedural Trays with Sterile Blades May Have Damaged Packaging
Medline Industries is recalling 45 units of procedural trays containing sterile surgical blades. The sharp blades may puncture the outer sterile packaging, potentially compromising sterility and increasing infection risk.
Product
Non-sterile procedural trays labeled as THEDA CLARK TOTAL KNEE CDS, 1 per case
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1033-2023·2023-02-08
Non-sterile orthopedic procedural trays recalled for potential sterile packaging breach
Medline Industries recalls non-sterile orthopedic procedural trays that may contain sterile blades capable of puncturing the protective foil packaging, compromising sterile barriers.
Product
Non-sterile procedural trays labeled as ORTHO TRAUMA, 1 per case
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1026-2023·2023-02-08
Affinity Fusion Oxygenator adapter may loosen during cardiac surgery
Medtronic is recalling Affinity Fusion Oxygenators because the Temperature Monitoring Adapter may come loose during setup or disassembly of the heart-lung machine used in cardiac surgery. No injuries have been reported.
Product
Affinity Fusion Oxygenator with Integrated Arterial Filter and Balance Biosurface, Custom Packs, REF CB841. Used in Cardiopulmonary bypass.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1036-2023·2023-02-08
OSS Modular Arthrodesis Nail Recalled for Missing Locking Bolts
Biomet is recalling certain OSS Modular Arthrodesis Nails due to missing locking bolts that could require extended surgery. Affected units are Lot 136620.
Product
OSS Modular Arthrodesis Nail, 7 Degree Collar Assembly with Locking Bolts-For use in the replacement of segmental defects of long bone, including midshaft replacement, and arthrodesis of the knee Item Number: CP260602
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0330-2023·2023-02-08
Alpha Plant-Based Burrito Recall: Undeclared Milk Allergen
THE MISO BROTHERS INC is recalling Alpha Plant-Based Burritos because they contain undeclared milk, a common allergen. Approximately 31,092 units are affected across US retail locations.
Product
Alpha Plant-Based Burrito - Philly 5.5 oz UPC 855099007023 Frozen
Category
Food
Distribution
0 states
HighFDA (Food)·F-0334-2023·2023-02-08
Ube Spanish Bread Recalled Due to Undeclared Wheat Allergen
Joy Joys Bakery LLC recalls Ube Spanish Bread because the label lists 'flour' without specifying it is wheat flour, failing to disclose a major allergen. The product was distributed in Washington and Oregon.
Product
Ube Spanish Bread, UPC 36897113. Product is packaged in plastic clear clamshell container and there are 6 pieces per container. Ingredients: Ube Flavoring, Butter, Egg, Flour, Water, Milk, Sugar, Salt, Yeast. Joy Joy s Bakery contact information: (253) 507-5259, 11107 Pacific…
Category
Food
Distribution
2 states
HighFDA (Food)·F-0331-2023·2023-02-08
Frozen burritos recalled for undeclared milk allergen
THE MISO BROTHERS INC is recalling Alpha Plant-Based Burrito (Pizza, 5.5 oz) because the product contains undeclared milk. Consumers with milk allergies should not consume this product.
Product
Alpha Plant-Based Burrito - Pizza 5.5 oz UPC 855099007016 Frozen
Category
Food
Distribution
0 states
HighFDA (Devices)·Z-1024-2023·2023-02-08
Affinity Fusion Oxygenator temperature monitoring adapter may loosen during cardiac surgery
The temperature monitoring adapter on Medtronic's Affinity Fusion Oxygenator may come loose during cardiopulmonary bypass procedures. The manufacturer has received multiple complaints about this issue.
Product
Affinity Fusion Oxygenator with Integrated Arterial Filter and Balance Biosurface, OXY/CVR COMBO BB841 FUSION W/BALANCE 26L, REF BB841. Used in Cardiopulmonary bypass.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0328-2023·2023-02-08
Frozen Plant-Based Breakfast Sandwich Recalled for Undeclared Milk Allergen
THE MISO BROTHERS INC is recalling Alpha Plant-Based Breakfast Sandwiches because they contain milk that is not listed on the label. Consumers with milk allergies may experience allergic reactions.
Product
Alpha Plant-Based Breakfast Sandwich - Meatless Spicy Chorizo, Plant-Based Egg & Cheeze 5 oz UPC 810070350109 Frozen
Category
Food
Distribution
0 states
HighFDA (Food)·F-0336-2023·2023-02-08
Ube Roll bakery product recall due to undeclared wheat allergen
Joy Joys Bakery is recalling Ube Roll packages because the label lists 'flour' but does not specify it is wheat flour, creating an allergen risk for consumers with wheat sensitivity.
Product
Ube Roll UPC 35961092. Product is packaged in plastic clear clamshell container and there are 3 pieces per container. Ingredients: Ube Flavoring, Butter, Flour, Sugar, Salt, Yeast, Egg, Milk, Water. Joy Joy s Bakery contact information: (253) 507-5259, 11107 Pacific HWY SW…
Category
Food
Distribution
2 states
HighFDA (Devices)·Z-1051-2023·2023-02-08
Bard Catheter Repair Kits Recalled for Hardened, Unusable Adhesive
Bard Peripheral Vascular is recalling multiple catheter repair kits because the adhesive may be hardened or coagulated, rendering the kits unusable. Approximately 7,520 units were distributed worldwide.
Product
Catalog Number / Product Description 0601600 2.7F Broviac CV Catheter Repair Kit 0601610 4.2 Fr Broviac CV Catheter Repair Kit 0601620 6.6F Broviac CV Catheter Repair Kit 0601630 9.6F Hickman CV Catheter Repair Kit 0601680 Hickman / Leonard CV Catheter Repair Kit (all…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0318-2023·2023-02-08
DR SNACK Crystal Ginger recalled for undeclared sulfites
DR SNACK Crystal Ginger was recalled because the product contains undeclared sulfites. Affected products were distributed in the Northeast U.S.
Product
DR SNACK brand Crystal Ginger; Net Wt. 7.00 oz (0.20kg); Net 6oz; and Net 10 oz.
Category
Food
Distribution
7 states

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25751–25775 of 114516