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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10301–10325 of 36631

  • CriticalFDA (Food)·F-0174-2021·2020-12-16

    Hy-Vee Pot Roast Mix Recalled for Listeria Contamination

    Hy-Vee is recalling Short Cuts Pot Roast Mix because an ingredient tested positive for Listeria monocytogenes. Consumers should discard the product.

    Product
    Hy-Vee, Short Cuts, Pot Roast Mix sold by weight in approximate 1 lb containers, Distributed by Hy-Vee Inc, West Des Moines, IA UPC 272083 XXXXXX
    Category
    Food
    Distribution
    8 states
  • CriticalFDA (Food)·F-0173-2021·2020-12-16

    Hy-Vee Grill Ready Veggie Mix Recalled for Listeria

    Hy-Vee is recalling Short Cuts Grill Ready Veggie Mix because an ingredient tested positive for Listeria monocytogenes.

    Product
    Hy-Vee, Short Cuts, Grill Ready Veggie Mix sold by weight in approximate 1 lb containers, Distributed by Hy-Vee Inc, West Des Moines, IA UPC 272104 XXXXXX
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Drugs)·D-0125-2021·2020-12-16

    FDA Recalls Imatinib Mesylate Tablets Due to Manufacturing Deviations

    Shilpa Medicare Limited is recalling 4,166 bottles of Imatinib Mesylate 400 mg tablets nationwide due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    IMATINIB MESYLATE — IMATINIB MESYLATE (IMATINIB MESYLATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V787000·2020-12-16

    2021 Thomas Built Saf-T-Liner C2 Electric School Bus Brake Recall

    Daimler Trucks North America is recalling 28 electric school buses where the parking brake may release unexpectedly, increasing crash risk.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0161-2021·2020-12-16

    Prairie Farms Chocolate Milk Recalled for Undeclared Egg

    Prairie Farms is recalling 355 gallons of chocolate milk sold in the Chicago area due to undeclared egg.

    Product
    Prairie Farms Premium Flavored Chocolate Milk, 1 gallon, UPC 72730-26110
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0179-2021·2020-12-16

    Fresh Attitude Baby Spinach Recalled for Potential Salmonella Contamination

    Veg Pro International Inc. is recalling Fresh Attitude Baby Spinach due to potential Salmonella contamination. The product was distributed across several Northeastern and Mid-Atlantic states.

    Product
    1. Fresh Attitude Baby Spinach, 11 oz. 2. Fresh Attitude Baby Spinach, 5 oz.
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Drugs)·D-0120-2021·2020-12-16

    Fresenius Kabi Recalls Dexmedetomidine Injection Due to Lidocaine Contamination

    Fresenius Kabi is recalling 13,525 bottles of Dexmedetomidine HCl Injection due to cross-contamination with trace amounts of lidocaine.

    Product
    Dexmedetomidine HCl in 0.9% Sodium Chloride Injection, 200 mcg / 50 mL (4 mcg / mL), 50 mL Single Dose Bottle, Rx only, Fresenius Kabi, Lake Zurich, IL 60047, NDC 63323-671-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0126-2021·2020-12-16

    Shilpa Medicare Recalls Docetaxel Injection Due to Manufacturing Deviations

    Shilpa Medicare Limited is recalling 2,008 vials of Docetaxel Injection USP due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    Docetaxel Injection USP 160 mg/8mL (20 mg/mL), For Intravenous Infusion Only, Rx Only, 8 mL Single Use Vial, Cytotoxic Agent, Manufactured by: Shilpa Medicare Limited, India, Distributed by: Armas Pharmaceuticals, Inc., Manalapan, NJ 07726, NDC 72485-216-08.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0121-2021·2020-12-16

    Shilpa Medicare Recalls Busulfan Injection Due to Manufacturing Deviations

    Shilpa Medicare Limited is voluntarily recalling 2,064 vials of Busulfan Injection due to CGMP deviations. The recall is nationwide and the lot expired in December 2020.

    Product
    Busulfan Injection 60 mg/10 mL (6 mg/mL), For Intravenous Infusion Only, Must be diluted before use, Single Dose Vial, Sterile, Cytotoxic Agent, Rx Only, 10 mL vial, Manufactured by: Shilpa Medicare Limited, India, Distributed by: Armas Pharmaceuticals, Inc., Manalapan, NJ 07726,
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0123-2021·2020-12-16

    Shilpa Medicare Recalls Azacitidine Injection Vials Due to Manufacturing Deviations

    Shilpa Medicare Limited is recalling 6,560 vials of Azacitidine for Injection due to Current Good Manufacturing Practice (CGMP) deviations. The recall is voluntary and nationwide.

    Product
    Azacitidine for Injection 100 mg/vial, For Subcutaneous and Intravenous Use Only, Rx Only, One Single Dose Vial, Cytotoxic Agent, Manufactured by: Shilpa Medicare Limited, India, Distributed by: Armas Pharmaceuticals, Inc., Manalapan, NJ 07726, NDC 72606-558-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V785000·2020-12-16

    Volkswagen Recalls 2012-2014 Beetles for Air Bag Inflator Defect

    Volkswagen is recalling 2012-2014 Beetle and Beetle Convertible vehicles because the driver's side air bag inflator may explode due to propellant degradation.

    Product
    VOLKSWAGEN — VOLKSWAGEN BEETLE CONVERTIBLE, BEETLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·21055·2020-12-16

    LG Energy Solution Recalls Home Batteries Due to Fire Hazard

    LG Energy Solution Michigan is recalling about 1,815 RESU 10H home batteries because they can overheat and cause fires. Consumers should contact the company for a free replacement.

    Product
    LG Chem "RESU 10H" Lithium-Ion Residential Energy Storage System
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0168-2021·2020-12-16

    Whole Foods Market Recalls Popcorn Chicken Shaker with Sweet Chili

    Whole Foods Market is recalling Popcorn Chicken Shaker with Sweet Chili due to undeclared shrimp allergen.

    Product
    Whole Foods Market Popcorn Chicken Shaker with Sweet Chili Variable weight sold by lb. Packed For Whole Foods Market
    Category
    Food
    Distribution
    2 states
  • SevereNHTSA·20V786000·2020-12-16

    Audi Recalls 2020 Q3 Vehicles Due to Brake Pedal Plate Defect

    Volkswagen Group of America is recalling 2020 Audi Q3 vehicles because the brake pedal plate can bend or detach, increasing crash risk.

    Product
    AUDI — AUDI Q3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0117-2021·2020-12-16

    FDA Recalls Protz Antibacterial Hand Sanitizer for CGMP Violations

    Asiaticon, SA de CV is recalling 111,500 units of Protz Antibacterial Hand Sanitizer distributed in Texas due to a lack of Current Good Manufacturing Practices (CGMPs).

    Product
    Protz real protection Antibacterial Hand Sanitizer, Ethyl Alcohol 70%, 13.5 FL OZ (400 mL), Distributed by: Safety-Med Products, Inc. Burlington, WI 53105 Made in Mexico by Asiaticon S.A. de C.V. Conkal No. 62, Mexico, Ciudad de Mexico 14200, Mexico NDC: 75192-600-02 UPC 7 503019
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Food)·F-0169-2021·2020-12-16

    Golden Boy Custard Muffins Recalled for Undeclared Milk and Dye

    Hong Thai Foods Corp is recalling Golden Boy Custard Muffins Original due to undeclared milk and Uranine-Acid Yellow 73.

    Product
    Golden Boy brand Custard muffin Original; 7.76 ounce, rigid clear plastic packages
    Category
    Food
    Distribution
    4 states
  • SevereNHTSA·20V782000·2020-12-15

    2021 Volvo Truck Air Brake Line Defect Recall

    Volvo Trucks is recalling 6,982 commercial trucks (2021 VHD, VNL, VNR, and VAH models) because damaged collets in the air brake system may cause park brakes to apply unexpectedly, potentially causing loss of vehicle control.

    Product
    VOLVO — VOLVO VAH, VNL, VHD, VNR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V780000·2020-12-15

    Certain Jayco and Entegra Motorhomes Leveling System Support Bracket Defect Recall

    Jayco and Entegra are recalling certain 2020-2021 motorhomes with defective leveling system support brackets that may fail, allowing components to contact the ground and potentially leak hydraulic fluid, increasing crash risk.

    Product
    JAYCO — JAYCO, ENTEGRA REDHAWK, REDHAWK SE, GREYHAWK, ESTEEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V776000·2020-12-11

    Mercedes-Benz Recalls AMG GLC63 Vehicles Due to Starter Cable Defect

    Mercedes-Benz is recalling 2,563 AMG GLC63 vehicles because a starter cable may chafe and short-circuit, increasing the risk of a stall or fire.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG GLC63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V772000·2020-12-11

    Mercedes-Benz Recalls One 2019 Sprinter 2500 for Hood Installation Defect

    Daimler Vans USA is recalling one 2019 Mercedes-Benz Sprinter 2500 because the engine hood may not have been installed properly, posing an injury risk in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ SPRINTER 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V774000·2020-12-11

    Kawasaki Recalls 2021 Ninja 400 and Z400 Motorcycles for Engine Defect

    Kawasaki is recalling 2021 Ninja 400 and Z400 motorcycles because a weak camshaft chain tensioner could cause the engine to stall, increasing crash risk.

    Product
    KAWASAKI — KAWASAKI NINJA 400, EX400G, Z400
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20E091000·2020-12-11

    Ohlins Recalls Front Struts for Porsche 911 Models Due to Pin Breakage Risk

    Ohlins is recalling front struts for specific Porsche 911 models because the strut pin may break during maximum steering, potentially causing loss of vehicle control.

    Product
    PORSCHE — PORSCHE 911 CARRERA, 911 TURBO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V765000·2020-12-10

    Altec Recalls 2018-2020 Digger Derricks Due to Hydraulic Valve Defect

    Altec is recalling 2018-2020 digger derricks and aerial devices because a hydraulic check valve snap ring can fail, causing unintended boom movement.

    Product
    ALTEC — ALTEC DIGGER DERRICK, AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide