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

13001–13025 of 31489

SevereFDA (Food)·F-1367-2024·2024-06-19
FDA Recalls Grande Ultra Whey Protein Isolate for Possible Salmonella
GRANDE CHEESE COMPANY is recalling Grande Ultra 9100 Functional Whey Protein Isolate (SKU 32131) due to possible Salmonella contamination. The recall affects 1.7 million pounds distributed to 24 U.S. states and international markets.
Product
Grande Ultra 9100 Functional Whey Protein Isolate. SKU 32131. 90% Protein. Grade A. Pasteurized. Net Wt 20 kg. Ingredients: Whey Protein Isolate Contains Milk. Grande Custom Ingredients Group, 250 Camelot Drive, Fond du Lac, WI
Category
Food
Distribution
24 states
SevereFDA (Food)·F-1347-2024·2024-06-19
Mt. Capra Goat Milk Formula Kit Recalled for Lack of FDA Premarket Notification
Mt. Capra Goat Milk Formula Recipe Kit recalled for marketing as infant formula without FDA premarket notification.
Product
Mt. Capra Goat Milk Formula Recipe Kit (net wt. 10lbs. 8oz.) and Bundle Refill. Each Goat Milk Formula Recipe Kit consist of 10 individually packaged ingredients: *Whole Goat Milk *Goat Milk Lactose *Goat Milk Ghee -Extra Virgin Olive Oil -Expeller-Pressed Grapeseed Oil
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1341-2024·2024-06-19
Irvington Seafood Jumbo Crab Meat recalled for Listeria contamination
Irvington Seafood is recalling Jumbo Crab Meat due to Listeria monocytogenes found during product testing. Affected packages distributed in Mississippi and Alabama should not be consumed.
Product
Irvington Seafood Jumbo Crab Meat packaged in 1 lb plastic cups. 40 lbs cases
Category
Food
Distribution
2 states
SevereFDA (Food)·F-1368-2024·2024-06-19
Whey Protein Isolate Recalled for Possible Salmonella Contamination
Grande Cheese Company is recalling Grande Ultra 8000 Nutritional Whey Protein Isolate due to possible Salmonella contamination. The affected batches include AOE813-1 through AOE813-4 and AOF840-1 through AOF840-4.
Product
Grande Ultra 8000 Nutritional Whey Protein Isolate. SKU 32200. 80% Protein Dry Basis. Grade A. Pasteurized. Net Wt 20 kg. Ingredients: Whey Protein Concentrate Contains Milk. Grande Custom Ingredients Group, 250 Camelot Drive, Fond du Lac, WI
Category
Food
Distribution
24 states
SevereFDA (Food)·F-1344-2024·2024-06-19
Claw Crab Meat Recall Due to Listeria Contamination
Irvington Seafood is recalling claw crab meat due to Listeria monocytogenes contamination found during product testing. The affected product was distributed in Mississippi and Alabama.
Product
Irvington Seafood Claw Crab Meat packaged in 1lb plastic cups. 40 lb cases
Category
Food
Distribution
2 states
SevereFDA (Drugs)·D-0553-2024·2024-06-19
Docetaxel Injection Recalled Due to Particulate Matter in Stopper
Sagent Pharmaceuticals is recalling Docetaxel Injection due to particulate matter from the vial stopper. Lot F1040001 was distributed nationwide.
Product
DOCETAXEL — DOCETAXEL (DOCETAXEL ANHYDROUS)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-1365-2024·2024-06-19
Grande Bravo Whey Protein Recalled Due to Salmonella Contamination
Grande Bravo 550 Functional Whey Protein is being recalled due to possible Salmonella contamination. Affected batches ANV508-1 and ANV508-3 were distributed across 24 U.S. states and internationally.
Product
Grande Bravo 550 Functional Whey Protein SKU 32105. 34% Protein. Grade A. Pasteurized. Net Wt 50 lbs. Ingredients: Whey Protein Concentrate Contains Milk. Grande Custom Ingredients Group, 250 Camelot Drive, Fond du Lac, WI
Category
Food
Distribution
24 states
SevereFDA (Food)·F-1369-2024·2024-06-19
Whey Protein Isolate Recalled Due to Possible Salmonella Contamination
Grande Ultra 9150 Whey Protein Isolate (Product Code 32324) is being recalled due to possible Salmonella contamination. The affected product was distributed to 24 US states and internationally to Canada, Ecuador, and Japan.
Product
Grande Ultra 9150 Whey Protein Isolate. Product Code: 32324. 90% Protein. Grade A. Pasteurized. Net Wt 20 kg. Ingredients: Whey Protein Isolate Contains Milk. Manufactured By: Grande Custom Ingredients Group, 1007 West Lake Street, Friendship, WI 53934.
Category
Food
Distribution
24 states
SevereFDA (Food)·F-1363-2024·2024-06-19
Grande Bravo 300 Whey Protein Recalled for Possible Salmonella Contamination
Grande Cheese Company is recalling Grande Bravo 300 Functional Whey Protein (SKU 32102) due to possible Salmonella contamination. The affected product was distributed across multiple US states and internationally.
Product
Grande Bravo 300 Functional Whey Protein SKU 32102. 34% Protein. Grade A. Pasteurized. Net Wt 50 lbs. Ingredients: Whey Protein Concentrate Contains Milk. Grande Custom Ingredients Group, 250 Camelot Drive, Fond du Lac, WI
Category
Food
Distribution
24 states
SevereFDA (Food)·F-1351-2024·2024-06-19
Newly Weds Foods Breader Mix Recalled for Potential Salmonella Contamination
Newly Weds Foods, Inc. is recalling 50-pound bags of breader (lot CD032324M) due to potential Salmonella contamination in an ingredient. The product was distributed to customers in Florida, Illinois, and Texas.
Product
Newly Weds Foods, LLC E50792 Breader X1 50lb bag
Category
Food
Distribution
3 states
SevereFDA (Food)·F-1349-2024·2024-06-19
Steak and Burger Seasoning Recalled by Newly Weds Foods for Potential Salmonella
Newly Weds Foods is recalling G51904 Steak and Burger Seasoning due to potential Salmonella contamination in an ingredient. Approximately 4,685 pounds were distributed to Florida, Illinois, and Texas.
Product
Newly Weds Foods, LLC G51904 Steak and Burger Seasoning 5lb. case
Category
Food
Distribution
3 states
SevereFDA (Food)·F-1346-2024·2024-06-19
Cup Saimin-Noodles recalled for undeclared egg allergen
H & U Inc. dba Sun Noodle is recalling S&S Cup Saimin-Noodles because the product contains undeclared egg, a major allergen. Approximately 39,522 cases were distributed in Hawaii, California, Nevada, and Utah.
Product
S&S Cup Saimin-Noodles with Soup & Garnish, NET WT. 5 oz., UPC 085315089056 and 085315089070
Category
Food
Distribution
4 states
SevereFDA (Food)·F-1343-2024·2024-06-19
Irvington Seafood Finger Crab Meat Recalled for Listeria Contamination
Irvington Seafood is recalling Finger Crab Meat due to Listeria monocytogenes contamination identified during product testing. The recall affects 168 lbs distributed in Mississippi and Alabama.
Product
Irvington Seafood Finger Crab Meat packaged in 1 lb plastic cups. 40 lbs cases
Category
Food
Distribution
2 states
SevereFDA (Devices)·Z-1921-2024·2024-06-19
Thoratec HeartMate System Monitor display malfunction in left ventricular assist devices
The Thoratec HeartMate System Monitor is being recalled due to display malfunctions affecting 4,842 devices worldwide. These issues may prevent proper monitoring and device control.
Product
Thoratec HeartMate System Monitor, REF: 1286, L1286, 1286A, L1286A, 1286A-US, L1286A-US, 1286C, L1286C, L1386, 1286A-CAN, 1286INT and L1286INT. Left ventricular assist device
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1355-2024·2024-06-19
Food ingredient recalled due to potential Salmonella contamination in Sun Nat product
Kerry Ingredients is recalling 13,341 bags of Sun Nat HV CHDR #3 SEAS food ingredient due to potential Salmonella contamination. No illnesses have been reported.
Product
Sun Nat HV CHDR #3 SEAS, Net Weight: 50.00 lb (22.68kg) SAP Code: 20737199. Kerry Ingredients, 3400 Millington Road, Beloit, WI 53511
Category
Food
Distribution
8 states
SevereFDA (Food)·F-1362-2024·2024-06-19
Grande Bravo Whey Protein Recalled for Possible Salmonella Contamination
Grande Cheese Company is recalling Grande Bravo 250 Functional Whey Protein (SKU 32101) for possible Salmonella contamination. The recall affects 1,726,910 pounds distributed across 24 U.S. states and exported to Canada, Ecuador, and Japan.
Product
Grande Bravo 250 Functional Whey Protein SKU 32101. Grade A. Pasteurized. Net Wt 50 lbs. Ingredients: Whey Protein Concentrate Contains Milk. Grande Custom Ingredients Group, 250 Camelot Drive, Fond du Lac, WI
Category
Food
Distribution
24 states
SevereFDA (Food)·F-1342-2024·2024-06-19
Irvington Seafood Lump Crab Meat Recalled Due to Listeria Contamination
Irvington Seafood, Inc. is recalling Lump Crab Meat due to Listeria monocytogenes contamination identified in finished product testing. The recalled product was distributed in Mississippi and Alabama.
Product
Irvington Seafood Lump Crab Meat packaged in 1 lb plastic ups. 40 lb cases
Category
Food
Distribution
2 states
SevereFDA (Food)·F-1356-2024·2024-06-19
Salt & Vinegar Seasoning Recalled Due to Potential Salmonella Contamination
Kerry, Inc has recalled Salt & Vinegar seasoning product due to potential Salmonella contamination. The affected product was distributed in multiple U.S. states and Canada.
Product
Salt & Vinegar 620592 Net Weight: 50lb (22.68kg) SAP Code: 20644388. Kerry Ingredients, 3400 Millington Road, Beloit, WI 53511
Category
Food
Distribution
8 states
SevereFDA (Food)·F-1350-2024·2024-06-19
Newly Weds Foods Starch WPC Blend Ingredient Recall Due to Salmonella
Newly Weds Foods, Inc. is recalling Starch WPC Blend 30lb bags due to potential Salmonella contamination in the ingredient. The recall affects 4,020 pounds of product distributed in Florida, Illinois, and Texas with lot numbers MT712282 and MT712283.
Product
Newly Weds Foods, LLC S07548 Starch WPC Blend 30lb bag
Category
Food
Distribution
3 states
HighFDA (Devices)·Z-2039-2024·2024-06-19
Coviden Monoject 60ml Syringes Recalled for Inadvertent Distribution
Coviden Monoject 60ml Luer-Lock syringes were inadvertently distributed despite being quarantined. Mckesson Medical-Surgical is recalling approximately 100 units (lot 330737X) distributed in the United States.
Product
Coviden Monoject 60ml Syringe Luer-Lock Tip-used to inject fluid into or withdraw fluids from the body MMS Catalog Number: 1159851 Cardinal Catalog Number: 8881560125
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2137-2024·2024-06-19
CODMAN EVD BACTISEAL Catheter Sterile Packaging Defect Recall
Integra LifeSciences recalls CODMAN EVD BACTISEAL catheters due to defects in sterile packaging that may compromise product sterility. The defect affects 106 units distributed worldwide.
Product
CODMAN EVD BACTISEAL 1.9mm I.D. Catheter Set- indicated for gaining access to the ventricles of the brain and can be used with dimensionally compatible devices for draining cerebrospinal fluid (CSF) and other fluids of similar physical characteristics as a means of reducing intra
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2142-2024·2024-06-19
VITROS Immunodiagnostic Calibrators Recalled for Potential Accuracy Bias
Ortho-Clinical Diagnostics is recalling VITROS Anti HBs Calibrators due to potential for positively biased results caused by signal reduction over shelf life. Approximately 481 units were distributed worldwide.
Product
VITROS Immunodiagnostic Products Anti HBs Calibrators. The VITROS Anti-HBs Calibrator Pack contains 3 X labelled Calibrator tube (1 per level: C1 - green, C2 - yellow, C3 - red).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1358-2024·2024-06-19
Jamai Bou Chanachur Snack Mix Recalled for Undeclared Peanuts
Jamai Bou CHADNI HOT MIX CHANACHUR snack is being recalled because peanuts are present but not declared on the label. This poses a serious risk to consumers with peanut allergies.
Product
Jamai Bou CHADNI HOT MIX CHANACHUR, 300 g (10.5 oz) bag, UPC 8 904293 104129, 30 bags per wholesale case
Category
Food
Distribution
3 states
HighFDA (Drugs)·D-0546-2024·2024-06-19
Zilretta Injectable Drug Recalled for Failed Stability Specifications
Pacira Pharmaceuticals is recalling 43,768 kits of Zilretta injectable suspension due to failed stability specifications at 2–8°C storage for 12 months followed by 25°C for 6 weeks. No illnesses or injuries have been reported.
Product
ZILRETTA — ZILRETTA (TRIAMCINOLONE ACETONIDE EXTENDED-RELEASE INJECTABLE SUSPENSION)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0548-2024·2024-06-19
FDA Recalls Eye Suspension Medication for Lack of Sterility Assurance
Imprimis NJOF, LLC is recalling one lot of a compounded ophthalmic suspension due to failure of sterility assurance. The product may be contaminated and pose a risk of serious eye infection.
Product
Prednisolone-Moxifloxacin-Bromfenac Sterile Ophthalmic Suspension, 1%, 0.5%, 0.075%, 5mL, Quantity: 20mL, Rx Only, Compounded by: Imprimis NJOF, LLC. 1705 Route 46 West, Unit 6B Ledgewood, NJ NDC 71384-310-05
Category
Drug
Distribution
Distributed nationwide

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13001–13025 of 31489