The Recall Desk

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.

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12126–12150 of 27719

  • 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 (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-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-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-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-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-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-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-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-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 (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-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-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-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-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-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
  • 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
  • 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-0547-2024·2024-06-19

    Klarity-C Ophthalmic Emulsion Recalled Due to Sterility Assurance Risk

    Imprimis is recalling Klarity-C, a cyclosporine eye medication, because the company cannot assure the product meets sterility standards. Approximately 136,005 units were distributed nationwide.

    Product
    Klarity-C (cyclosporine) Preservative-Free Sterile Ophthalmic Emulsion 0.1% 5.5mL, Rx Only, This is a compounded drug. NOT FOR RESALE. OFFICE USE ONLY Compounded by: Imprimis NJOF, LLC., 1705 Route 46 West, unit 6B, Ledgewood, NJ 07852 NDC: 71384-514-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2135-2024·2024-06-19

    CORI Surgical System Software Error Causes Tracking Array Flickering

    The CORI Starter Kit surgical system may experience display flickering from a software tracking error, potentially causing surgical delays during orthopedic procedures.

    Product
    CORI Starter Kit, Real Intelligence CORI, CORI STARTER KIT - UNIVERSAL.Intended to assist the surgeon in providing software-defined spatial boundaries for orientation and reference information to anatomical structures during orthopedic procedures Product Numbers: (1) ROB10000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • 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-2033-2024·2024-06-19

    Streptococcal A Rapid Test Kits Recalled for Unauthorized Distribution

    Wondfo USA is recalling 102,500 units of IMCO Strep A Rapid Test Kits due to unauthorized distribution for at-home, over-the-counter, and direct-to-consumer use.

    Product
    Independent Medical Co-op Inc., Streptococcal A rapid test kits, labeled as: IMCO Strep A Rapid Test Strip and IMCO Strep A Rapid Test, Part Number STP25-IMC
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2138-2024·2024-06-19

    EVD Catheter Sterile Packaging Defect Recall for Intracranial Drainage

    Integra LifeSciences is recalling CODMAN BACTISEAL EVD catheters due to external packaging seal defects that may compromise sterility. The recall affects 59 units distributed internationally.

    Product
    CODMAN BACTISEAL Clear EVD Catheter 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
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2133-2024·2024-06-19

    Stimuplex A Anesthesia Needles Recalled for Undisclosed DEHP in Glue

    B Braun Medical Inc is recalling 108,811 units of Stimuplex A anesthesia needles because the devices are labeled as DEHP-free but the glue contains traces of DEHP.

    Product
    Stimuplex A, 30 DEG, 20GX6", 0.90x150mm, Catalogue Number: 4894278
    Category
    Medical Device
    Distribution
    Distributed nationwide