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

4976–5000 of 7171

SevereFDA (Devices)·Z-1147-2023·2023-03-15
Cardiosave Hybrid IABP Recalled for Risk of Unexpected Shutdown
The Cardiosave Hybrid intra-aortic balloon pump (IABP) is being recalled because it may unexpectedly shut down due to communication loss between internal components. The shutdown could interrupt therapy in cardiac patients and compromise their hemodynamic stability.
Product
Cardiosave Hybrid Model Nos. 0998-00-0800-31 0998-00-0800-32 0998-00-0800-33 0998-00-0800-34 0998-00-0800-35 0998-00-0800-45 0998-00-0800-52 0998-00-0800-53 0998-00-0800-55 0998-00-0800-65 0998-UC-0800-31* 0998-UC-0800-33* 0998-UC-0800-52* 0998-UC-0800-53* 0998
Category
Medical Device
Distribution
Distributed nationwide
CriticalCPSC·23150·2023-03-09
Calico Critters Animal Figures Recalled Due to Choking Hazard; Two Deaths Reported
Epoch Everlasting Play is recalling more than 3.2 million Calico Critters animal figures and sets sold with bottle and pacifier accessories due to choking hazard. Two fatal incidents have been reported.
Product
Calico Critters® Animal Figures and Sets sold with Bottle and Pacifier Accessories
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·23735·2023-03-09
Bedsure Electric Heating Blankets and Pads Recalled for Fire and Burn Hazards
Bedsure electric heating blankets and pads are recalled because their controllers can malfunction, causing fires and thermal burns. Consumers should stop using them immediately and contact Bedsure for a refund.
Product
Bedsure Electric Heating Blankets and Pads
Category
Consumer Product
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0453-2023·2023-03-08
PrimeZEN Black 6000 Capsule Recalled for Undeclared Pharmaceutical Ingredients
The FDA is recalling PrimeZEN Black 6000 capsules distributed nationwide because they contain undeclared sildenafil and tadalafil. The product is unapproved and was marketed without FDA authorization.
Product
PrimeZEN Black 6000 capsule, 2000mg, Male Sexual Performance Enhancement, 1-count blister card, Distributed by: Prime Premier Group, Los Angeles, CA 90006, UPC 7 28175 52189 1.
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·23V155000·2023-03-08
Ford Recalls 2022-2023 Bronco for Steering Gear Lock-Up Defect
Ford recalls 2022-2023 Broncos for steering gear damage that can lock up the steering wheel and cause loss of steering control, increasing crash risk.
Product
FORD — 2022 FORD BRONCO
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1140-2023·2023-03-08
Life2000 Hospital Ventilator Recalled for Potential Patient Desaturation Risk
Baxter Healthcare is recalling 135 Life2000 ventilators nationwide due to potential patient desaturation when connected to an oxygen concentrator.
Product
Life2000 Ventilator PKG, Hospital, a) REF BT20007, b) REF BT-20-0007, ventilatory support for the care of individuals
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·23V154000·2023-03-08
2023-2024 International trucks recalled for loose battery box bolts
Navistar is recalling certain 2023 and 2024 International trucks because battery box mounting bolts may be loose or missing. Loose bolts could allow the battery box to detach, creating a road hazard and increasing crash risk.
Product
INTERNATIONAL — 2023 INTERNATIONAL MV
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1139-2023·2023-03-08
Life2000 Ventilator System Recall: Risk of Patient Desaturation
Baxter Healthcare is recalling 4,279 Life2000 Ventilator Systems due to potential patient desaturation when connected to oxygen concentrators.
Product
Life2000 Ventilator System, a) REF BT-20-0002, b) REF BT-20-0002A, ventilatory support for the care of individuals
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1141-2023·2023-03-08
Life2000 Hospital Ventilator Recalled for Patient Desaturation Risk
Baxter Healthcare is recalling 8 Life2000 Hospital Ventilator systems due to potential patient desaturation events when the device is connected to an oxygen concentrator.
Product
Life2000 Ventilator PKG, Hospital, a) REF BT200011, b) REF BT-20-0011, ventilatory support for the care of individuals
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1142-2023·2023-03-08
Life2000 Ventilator poses oxygen desaturation risk with oxygen concentrators
The FDA recalls Baxter's Life2000 Ventilator due to potential patient desaturation when connected to an oxygen concentrator. Affects 71 units nationwide.
Product
Life2000 Ventilator , REF MS-01-0118, ventilatory support for the care of individuals
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0384-2023·2023-03-08
Matsunaga Mini Shiruko Sand Biscuits Recalled Due to Undeclared Soy Allergen
Matsunaga Mini Shiruko Sand Biscuits are being recalled because they contain soy allergen that is not listed on the ingredient label. Consumers with soy allergies should not consume this product.
Product
Matsunaga Mini Shiruko Sand Biscuits 100 g packages, containing 4 individually wrapped servings of 4 (25mg per unit) SKU number 4902773016966 Manufactured in Japan.
Category
Food
Distribution
0 states
CriticalFDA (Food)·F-0370-2023·2023-03-01
Harvest Sesame Recalled for Undeclared Soy and Sesame Allergens
Daiso is recalling Harvest Sesame 94g units due to undeclared soy and sesame allergens on the label. The recall affects 317,751 units distributed across Daiso retail locations in six U.S. states and Canada.
Product
Harvest Sesame 94g units UPC:4901940041312
Category
Food
Distribution
5 states
CriticalFDA (Food)·F-0402-2023·2023-03-01
Ready-to-Eat Soup Recalled: Rao's Contains Undeclared Egg Allergen
Rao's Made for Home Slow Simmered Soup labeled as Chicken & Gnocchi is being recalled because it actually contains vegetable minestrone with an undeclared egg allergen. The recall affects 13,751 cases distributed across multiple states.
Product
Rao's Made for Home Slow Simmered Soup, labeled as Chicken & Gnocchi, Soup in 16-ounce glass jars, 6 jars per case. Shelf stable, refrigerate after opening.
Category
Food
Distribution
12 states
CriticalFDA (Food)·F-0371-2023·2023-03-01
Harvest Biscuits recalled for undeclared soy and peanut allergens
Harvest Biscuits 4Kinds of Nuts (94g units) are recalled because the product contains soy and peanuts that are not listed on the ingredient label. The product was distributed to Daiso stores across multiple US states and Canada.
Product
Harvest Biscuits 4Kinds of Nuts 94g units UPC:4901940041558
Category
Food
Distribution
5 states
CriticalFDA (Food)·F-0374-2023·2023-03-01
Daiso: Fly Beans Senbei cracker recall due to unlabeled peanuts
Daiso is recalling KASHIWADO Hitoritoiro Fly Beans Senbei because the product contains peanuts not listed on the label, creating a risk for consumers with peanut allergies.
Product
KASHIWADO Hitoritoiro Fly Beans Senbei UPC:4904036008213
Category
Food
Distribution
5 states
SevereFDA (Food)·F-0378-2023·2023-03-01
Daiso Potato Crackers with Sardines Recalled for Undeclared Milk
Daiso potato crackers with sardines (46g) are being recalled due to undeclared milk allergen. The product was distributed across six US states and parts of Canada.
Product
Potato crackers with small sardines 46g UPC: 4901053077376
Category
Food
Distribution
0 states
SevereFDA (Food)·F-0373-2023·2023-03-01
KASHIWADO senbei crackers recalled due to undeclared peanuts
KASHIWADO Hitoritoiro Fly Beans Senbei crackers are being recalled because the product contains peanuts that are not listed on the ingredient label. Consumers with peanut allergies should avoid this product.
Product
KASHIWADO Hitoritoiro Fly Beans Senbei UPC:4904036008213
Category
Food
Distribution
5 states
SevereFDA (Food)·F-0363-2023·2023-03-01
Pilgrim's Roasted Nut'Z Squirrel Mix recalled for undeclared milk and soy allergens
Pilgrim's Roasted Nut'Z Squirrel Mix (8 oz bags) is recalled for undeclared milk, soy lecithin, and food colors. The product poses allergic reaction risk to consumers with milk or soy allergies.
Product
Pilgrim's Roasted Nut'Z Squirrel Mix are packaged by hand into either the 8 oz Plastic Cone Bags or 8 Oz Pouch Bags. Label declares almonds, Spanish peanuts, mini M&M's, Golden Raisins, Sugar, Vanilla.
Category
Food
Distribution
0 states
SevereFDA (Food)·F-0359-2023·2023-03-01
Pilgrim's Roasted Nut'Z Chocolate Toffee Almonds recalled for undeclared milk and soy
Pilgrim's Roasted Nut'Z Chocolate Toffee Almonds are recalled due to undeclared milk and soy lecithin. The product poses a serious risk to consumers with dairy and soy allergies.
Product
Pilgrim's Roasted Nut'Z Chocolate Toffee Almonds are packaged by hand into either the 8 oz Plastic Cone Bags or 8 Oz Pouch Bags. Label declares Almonds, Sugar, Hershey's Cocoa Powder, Ghirardelli Sweet Chocolate Powder, English Toffee Syrup.
Category
Food
Distribution
0 states
SevereFDA (Food)·F-0379-2023·2023-03-01
ITOSEIKA Chocolate Chip Cookies Recalled for Undeclared Milk Allergen
DAISO CALIFORNIA WAREHOUSE is recalling ITOSEIKA Chocolate Chip Cookies due to undeclared milk allergen on the label. Products were distributed to Daiso stores in California, Washington, Nevada, Texas, New York, New Jersey, and British Columbia.
Product
ITOSEIKA Chocolate chip cookies 10pieces UPC: 4901050137172
Category
Food
Distribution
0 states
SevereFDA (Food)·F-0380-2023·2023-03-01
Katoseika Chocolat Orange Candy recalled for undeclared soy allergen
Daiso California Warehouse is recalling Katoseika Chocolat Orange Candy (60g) due to undeclared soy allergen. The product was distributed to Daiso stores across multiple U.S. states and Canada.
Product
Katoseika Chocolat Orange Candy 60g UPC: 4901580002315
Category
Food
Distribution
0 states
SevereFDA (Food)·F-0381-2023·2023-03-01
KANRO Pure Gummy Candy Recalled for Undeclared Soy Allergen
KANRO Pure gummy candies are being recalled due to undeclared soy allergen on the label. The recall affects 113,205 units sold at Daiso stores across multiple states and Canada.
Product
KANRO Pure gummy Petit trigonal pyramid grape 17g 3 pieces UPC: 4901351055489
Category
Food
Distribution
0 states
SevereFDA (Food)·F-0361-2023·2023-03-01
Pilgrim's Roasted Nut'Z English Toffee Peanuts recalled due to undeclared milk
Pilgrim's Roasted Nut'Z English Toffee Peanuts (580 packages) are recalled because the label does not declare the presence of milk. Consumers with milk allergies should not consume this product.
Product
Pilgrim's Roasted Nut'Z English Toffee Peanuts are packaged by hand into either the 8 oz Plastic Cone Bags or 8 Oz Pouch Bags. Label declares Spanish peanuts, sugar, English Toffee Syrup.
Category
Food
Distribution
0 states
SevereFDA (Devices)·Z-1137-2023·2023-03-01
NovaStar TS Anti-Asphyxia Valve recalled for magnetic interference risk
Draeger Medical recalls NovaStar TS Anti-Asphyxia Valves due to magnets that may interfere with implanted and non-implanted medical devices and metallic implants.
Product
NovaStar TS, Anti-Asphyxia Valve, Reusable, Material Numbers MP01576 (Size S), MP01577 (Size M), and MP01578 (Size L)
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0377-2023·2023-03-01
MEITO Powdered Apple Tea recalled for undeclared milk allergen
DAISO CALIFORNIA WAREHOUSE is recalling MEITO Powdered Apple Tea 4packs because the product contains milk that is not declared on the label. Consumers with milk allergies should not consume this product.
Product
MEITO Powdered Apple Tea 4packs UPC: 4902757413606
Category
Food
Distribution
0 states

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4976–5000 of 7171