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

19526–19550 of 27461

SevereFDA (Devices)·Z-0963-2023·2023-02-08
CADD Infusion Administration Sets Recalled for Tubing Occlusion and False Alarms
Smiths Medical is recalling CADD Administration Sets for two issues: tubing may become blocked, preventing medication delivery, and devices may show false alerts about disposable attachment status.
Product
CADD Administration Set, List Numbers: 1) REF 21-7300-24, 2) REF 21-7301-24 3) REF 21-7302-24, 4) REF 21-7321-24, 5) REF 21-7322-24, 6) REF 21-7323-24, 7) REF 21-7324-24, 8) REF 21-7333-24, 9) REF 21-7336-24, 10) REF 21-7339-24, 11) REF 21-7343-24, 12) REF 21-7349-24,
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0253-2023·2023-02-08
Easy Care First Aid Kit Recalled for Microbial Contamination
The FDA is recalling Easy Care First Aid kits containing After Burn Cream due to microbial contamination. The affected product was distributed nationwide and in Canada with lot number W06H15 (expiration August 15, 2024).
Product
Easy Care First Aid 10 Person 2009 ANSI, First Aid Kit, containing Easy Care first aid After Burn Cream 0.9 g packets, Product # 9999-2131
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0964-2023·2023-02-08
CADD Infusion Administration Sets Recalled for Delivery Failure and Alarms
FDA recalls 726,878 CADD Infusion Administration Sets due to potential tubing occlusion causing delivery failure and false alarm warnings.
Product
CADD Administration Set, List Numbers: a) REF 21-7308-24, b) REF 21-7309-24, c) REF 21-7310-24, d) REF 21-7308-24JP, e) REF 21-7309-24JP. Computerized Ambulatory Delivery Device
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0248-2023·2023-02-08
FDA Recalls Easy Care First Aid Kits for Bacterial Contamination
GFA Production's Easy Care First Aid 25 Person kits are being recalled nationwide due to contamination with Bacillus bacteria. The affected first aid cream packets could pose a risk if applied to open wounds.
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 # 9999-2129
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0324-2023·2023-02-08
Fullei Fresh Alfalfa Sprouts Recalled for Possible E. coli Contamination
Fullei Fresh brand alfalfa sprouts are recalled due to possible contamination with Shiga toxin-producing E. coli. The recall affects 333 cases distributed in Florida, lot number 336.
Product
Fullei Fresh brand Alfalfa Sprouts in a 4 oz. clear plastic clamshell container; UPC Code 17442 30012. Packaged in 5lb carboard box 12 packages of 4 oz
Category
Food
Distribution
1 state
SevereFDA (Food)·F-0338-2023·2023-02-08
Wegmans tiramisu products contain undeclared wheat
Wegmans bakery tiramisu products contain undeclared wheat not listed on the label. The products are marked as made with no gluten-containing ingredients but do not declare wheat as an allergen.
Product
Wegmans bakery Tiramisu, Half Tiramisu, and Tiramisu Slices; Made with No Gluten-Containing Ingredients; ALLERGENS: Contains Egg, Milk, Soy, Other allergens may be present due to shared preparation area.
Category
Food
Distribution
6 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
SevereFDA (Drugs)·D-0252-2023·2023-02-08
CVS First Aid Home Burn Cream Packets Recalled for Bacterial Contamination
CVS First Aid Home, First Aid Kit burn cream packets have been recalled due to bacterial contamination. The product contains Bacillus lichenformis and Bacillus sonorensis bacteria, creating a risk when applied to wounds or burns.
Product
CVS First Aid Home, First Aid Kit, containing Easy Care first aid After Burn Cream 0.9 g packets, Product # 2980-0700
Category
Drug
Distribution
Distributed nationwide
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 TES
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 (Devices)·Z-0965-2023·2023-02-08
CADD Infusion Administration Set Recalled for Delivery Failure and False Alarms
Smiths Medical is recalling CADD Administration Sets due to tubing occlusion that can prevent medication delivery and false pump alarms. This FDA Class I recall affects 214,668 units worldwide.
Product
CADD Administration Set, List Numbers: a) REF 21-7600-24, b) REF 21-7609-24, c) REF 21-7624-24, d) REF 21-7649-24, e) REF 21-7600-24JP, f) REF 21-7609-24JP, g) REF 21-7624-24JP, h) REF 21-7649-24JP Computerized Ambulatory Delivery Device
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-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-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 (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-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 (Devices)·Z-1044-2023·2023-02-08
Biopsy Medium for In Vitro Fertilization Recalled Due to Product Contamination
CooperSurgical is recalling a lot of Biopsy Medium used in IVF procedures because the product may contain an incorrect medium that could degrade embryos. No illnesses have been reported.
Product
BIOPSY MEDIUM 10ML, Reference Number 10620010 A, used for blastomere biopsy of cleavage stage embryos for Pre-implantation Genetic Diagnosis (PGD)
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1042-2023·2023-02-08
Vanguard Knee System Prosthesis Components Incorrectly Labeled for Size and Side
Biomet is recalling 157 units of Vanguard Knee System prosthesis components incorrectly labeled as different sizes or surgical sides. Surgeons relying on labels could implant the wrong size or side, requiring corrective surgery.
Product
(1) Vanguard Knee System PS Open Box Femoral; Right; 60 mm. Intended for knee joint replacement prostheses. Item Number: 183104 (2) Vanguard Knee System PS Open Box Femoral; Right; 62.5 mm Item Number: 183106 (3) Vanguard Knee System PS Open Box Femoral; Right; 65 mm Item Num
Category
Medical Device
Distribution
6 states
HighFDA (Devices)·Z-1038-2023·2023-02-08
Turbett Surgical Container TS1000 may have weld failures breaching sterile barrier
Turbett Surgical Container TS1000 may have weld failures that breach the sterile barrier, potentially resulting in unsterile instruments being used in medical procedures and risking patient infection or injury.
Product
Turbett Surgical Container, TS1000: Indicated for enclosing other medical devices that are to be sterilized by a healthcare provider
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0326-2023·2023-02-08
Plant-based breakfast burritos recalled for undeclared milk allergen
THE MISO BROTHERS INC is recalling 31,092 units of frozen Alpha Plant Based Breakfast Burritos due to undeclared milk. The product may contain milk, a common allergen.
Product
Alpha Plant Based Breakfast Burrito - Meatless Sausage SCRAMBLE 5.5 oz UPC 855099007733 Frozen
Category
Food
Distribution
0 states
HighFDA (Devices)·Z-1022-2023·2023-02-08
SynCardia Total Artificial Heart System Recalled for Cannula Tears
SynCardia Systems is recalling its Total Artificial Heart System due to reported tears in the cannula caused by wear and tear stress. Approximately 1,732 systems worldwide are affected.
Product
SynCardia Total Artificial Heart System (70CC): 500101-001 SynCardia Total Artificial Heart System (50CC): 570500-000
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1028-2023·2023-02-08
Medtronic Perfusion Oxygenator Temperature Monitoring Adapter Detachment Recall
Medtronic has recalled Custom Pack Perfusion Tubing Packs used in cardiopulmonary bypass procedures. The Temperature Monitoring Adapter on the oxygenator may detach during setup or disassembly.
Product
Custom Pack Perfusion Tubing Packs containing Affinity Fusion Oxygenator with Integrated Arterial Filter and Balance Biosurface, REF CB811. Used in Cardiopulmonary bypass.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1037-2023·2023-02-08
Turbett Surgical Container TS1200 Recalled Due to Potential Weld Failures
Turbett Surgical Container TS1200 units may have weld failures that could breach the sterile barrier, potentially allowing unsterile instruments to be used in medical procedures and risking infection.
Product
Turbett Surgical Container, TS1200: Indicated for enclosing other medical devices that are to be sterilized by a healthcare provider
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1047-2023·2023-02-08
Medline UNITE Foot & Ankle Drill Bit Recalled for Intra-operative Screw Failure Risk
Medline Industries recalls 190 UNITE foot and ankle drill bits due to observed screw failure during surgery. When used to pre-drill holes for certain screw sizes, the drill bits may fail under surgical torque, creating risk during procedures.
Product
MEDLINE UNITE FOOT & ANKLE DRILL BIT, 1.3MM Solid Core, REF MPN10013
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1032-2023·2023-02-08
Non-sterile procedural trays with potential sterile packaging breach
Medline Industries is recalling non-sterile procedural trays containing sterile blades that may damage sterile packaging due to blade puncture risk. Lot 22IBQ980. No illnesses reported.
Product
Non-sterile procedural trays labeled as MAJOR/MINOR, 3 per case
Category
Medical Device
Distribution
Distributed nationwide

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19526–19550 of 27461