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

12126–12150 of 27719

SevereFDA (Food)·F-1364-2024·2024-06-19
Whey Protein Powder Recalled for Possible Salmonella Contamination
Grande Bravo 500 Functional Whey Protein is recalled due to possible Salmonella contamination. The product was distributed across 24 US states and internationally to Canada, Ecuador, and Japan.
Product
Grande Bravo 500 Functional Whey Protein SKU 32103. 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-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
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-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-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-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 (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-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 (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 (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-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-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-1354-2024·2024-06-19
Seasoning Ingredient Recalled for Potential Salmonella Contamination
Kerry, Inc is recalling BrS8 RODIZIO Seas No MSG seasoning ingredient due to potential Salmonella contamination. The affected product was distributed to multiple U.S. states and Canada.
Product
BrS8 RODIZIO Seas No MSG 9.6#, SAP Code: 20644205. Kerry Ingredients, 3400 Millington Road, Beloit, WI 53511
Category
Food
Distribution
8 states
SevereFDA (Food)·F-1361-2024·2024-06-19
Grande Lactose ingredient recalled due to possible Salmonella contamination
Grande Lactose (SKU 30601) is being recalled due to possible Salmonella contamination. The affected product was distributed across multiple US states and internationally.
Product
Grande Lactose. SKU 30601. Grade A. Refined Pasteurized. Net Wt 25 kg. Ingredients: Lactose 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-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-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
HighFDA (Devices)·Z-2139-2024·2024-06-19
Aeos Robotic Digital Microscope recalled for safety mechanism failure
Aesculap Inc is recalling Aeos Robotic Digital Microscope models with Product Code PV010 due to failure of the integrated safety mechanism. The robotic arm may drop more than 10 cm from its original position after the emergency stop button is pressed.
Product
Aeos Robotic Digital Microscope, Product Code: PV010
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 (Devices)·Z-2134-2024·2024-06-19
Stimuplex A Nerve Needles Recalled for Mislabeled DEHP Content
B Braun Medical Inc is recalling over 1.1 million Stimuplex A nerve block needles labeled as DEHP-free, but the adhesive contains traces of DEHP. The mislabeling poses a risk to users who selected the product specifically to avoid DEHP exposure.
Product
Stimuplex A, 30 DEG, 22GX2", 0.70x50mm, Catalogue Number: 4894502
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0545-2024·2024-06-19
Prescription Drug Recall: Phenazopyridine Tablets Contain Wrong Medication
Winder Laboratories is recalling Phenazopyridine HCl tablets (Lot #1142404) due to a product mix-up where some bottles contain Phenobarbital tablets instead. No illnesses or injuries have been reported.
Product
PHENAZOPYRIDINE HYDROCHLORIDE — PHENAZOPYRIDINE HYDROCHLORIDE (PHENAZOPYRIDINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-1360-2024·2024-06-19
Grande Lactose SKU 30600 recalled for possible Salmonella contamination
Grande Cheese Company is recalling Grande Lactose SKU 30600 due to possible Salmonella contamination across 24 U.S. states and three countries. No illnesses have been reported.
Product
Grande Lactose SKU 30600. Grade A. Refined Pasteurized. Net Wt 25 kg. Ingredients: Lactose Contains Milk. Grande Custom Ingredients Group, 250 Camelot Drive, Fond du Lac, WI
Category
Food
Distribution
24 states
HighFDA (Devices)·Z-2141-2024·2024-06-19
Fresenius AquaA hemodialysis water purification device pressure control malfunction
Fresenius is recalling 4 hemodialysis water purification devices for pressure control malfunctions. When concentrate pressure exceeds the 19.9 bar limit, the device stops supplying water and halts dialysis treatment.
Product
US AquaA 900H-Typ USA-3 x 208v-Intended for the purification of water to be used for hemodialysis Vivonic Part Numbers: G02020110 Fresenius Part Number: 24-090A-1
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2041-2024·2024-06-19
MRI Systems Power Cable Terminal Block Fire Hazard Recall
Canon Medical MRI systems are being recalled because the terminal block securing the power cable may disconnect, potentially causing electrical arcing and fire. 153 units are affected across the United States and Puerto Rico.
Product
MRI systems: Vantage Orian MRT-1550 (MEXL-1550), Vantage Elan MRT-2020 (MEXL-1520), Vantage Titan MRT-1504 (MEXL-1504), Vantage Titan 3T MRT-3010 (MEXL-3010), Vantage Galan 3T MRT-3020 (MEXL-3020)
Category
Medical Device
Distribution
38 states
HighFDA (Drugs)·D-0549-2024·2024-06-19
Phenazopyridine bottles recalled due to medication mix-up error
RemedyRepack Inc. is recalling bottles labeled as Phenazopyridine HCl 100mg that actually contain Phenobarbital 16.2mg tablets. Eight bottles were distributed to one medical facility. Patients should not use these medications and must contact their healthcare provider.
Product
Phenazopyridine HCl, 100mg tablets, 6 count bottles, Rx Only, Repackaged by: RemedyRepack, Inc., Indiana, PA NDC#: 70518-0218-00, Source NDC: 75826-0114-10 MFG: Winder Laboratories, LLC, Winder, GA
Category
Drug
Distribution
0 states

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12126–12150 of 27719