The Recall Desk

Severity 4 of 5

Severe recalls

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

What “severe” means here

Severity 4 (Severe) recalls have a real, documented risk of significant injury, hospitalization, or property damage even if no deaths have been reported. The agency classification is FDA Class II with hospitalization reports, USDA Class I, or a structural vehicle defect. These need attention quickly — not five-alarm urgency but not something to put off. Examples include allergen mislabeling on common allergens for products eaten by children, drug potency out of specification by a margin that could cause measurable harm, and vehicle defects affecting braking or steering.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

8851–8875 of 29123

  • SevereUSDA FSIS·030-2020·2020-12-19

    Nestlé Recalls Lean Cuisine Baked Chicken Meals Due to Plastic Contamination

    Nestlé Prepared Foods is recalling Lean Cuisine Baked Chicken meal products that may contain pieces of hard white plastic. No illnesses have been reported.

    Product
    Nestlé Prepared Foods Recalls Lean Cuisine Baked Chicken Meal Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·029-2020·2020-12-19

    Perfect Pasta Recalls Frozen Meat and Poultry Products Lacking Federal Inspection

    Perfect Pasta Inc. is recalling frozen meat and poultry products produced without federal inspection. No adverse reactions have been reported.

    Product
    Perfect Pasta Inc. Recalls Frozen Meat and Poultry Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V793000·2020-12-17

    Land Rover Recalls 2020 Range Rover Evoque for Seat Belt Defect

    Jaguar Land Rover is recalling 2020 Range Rover Evoque vehicles because replacement second-row seat belts may not function properly in a crash.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER EVOQUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V792000·2020-12-17

    Chevrolet Silverado 1500 Front Seat Belt Brackets May Not Secure

    General Motors is recalling certain 2020 Chevrolet Silverado 1500 and other vehicles because front-row center seat belt brackets may not be properly secured to the seat frame, potentially preventing proper restraint in a crash.

    Product
    CHEVROLET — CHEVROLET, GMC SILVERADO 1500, SIERRA 2500, SILVERADO 3500, TAHOE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V791000·2020-12-17

    Ford Recalls Transit Connect and EcoSport for Air Bag Defect

    Ford is recalling 2019-2020 Transit Connect and 2020 EcoSport vehicles because air bag modules may lack first-stage booster propellant, preventing proper deployment in a crash.

    Product
    FORD — FORD TRANSIT CONNECT, ECOSPORT
    Category
    Vehicle
    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
  • 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
  • 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
  • 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
  • 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 (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
  • 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
  • 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 (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
  • 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-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 (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
  • 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 (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
  • 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 SE, GREYHAWK, ESTEEM, REDHAWK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • 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