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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10276–10300 of 36631

  • SevereCPSC·21058·2020-12-23

    Urban Outfitters Recalls Taper Candle Holders Due to Fire Hazard

    Urban Outfitters is recalling Swirled and Sofia Taper Candle Holders because they can catch fire if they contact a flame. Consumers should stop using them and return them for a refund.

    Product
    Swirled Taper and Sofia Taper Candle Holders
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0143-2021·2020-12-23

    Advanced Nutriceuticals Recalls LL-37 Vials Due to Sterility Concerns

    Advanced Nutriceuticals is recalling LL-37 vials because production processes cannot assure sterility. The product was distributed to seven states.

    Product
    LL-37, 2000 MCG/ML, 2 ML vial, The Guyer Institute of Molecular Medicine, Indianapolis, IN
    Category
    Drug
    Distribution
    7 states
  • SevereFDA (Drugs)·D-0137-2021·2020-12-23

    Advanced Nutriceuticals Recalls B12 Injection Vials Due to Sterility Concerns

    Advanced Nutriceuticals is recalling B12 for Injection vials because production processes cannot assure sterility. The product was distributed in seven states.

    Product
    B12 for Injection, 2 MG/ML, 10 ML vial, The Guyer Institute of Molecular Medicine, Indianapolis, IN
    Category
    Drug
    Distribution
    7 states
  • SevereFDA (Drugs)·D-0131-2021·2020-12-23

    FDA Recalls AOD-9604 Vials Due to Sterility Concerns

    Advanced Nutriceuticals, LLC is recalling AOD-9604 vials because production processes cannot assure sterility. The product was distributed in seven states.

    Product
    AOD-9604, 1200 MCG/ML, 5 ML vial The Guyer Institute of Molecular Medicine, Indianapolis, IN
    Category
    Drug
    Distribution
    7 states
  • SevereFDA (Devices)·Z-0576-2021·2020-12-23

    DePuy Synthes 12.5mm Reamer Head Recalled for Breakage and Tissue Damage

    Synthes (USA) Products LLC is recalling DePuy Synthes 12.5mm Reamer Heads for RIA 2 due to breakage exceeding expected rates, which can cause tissue and bone damage.

    Product
    DePuy Synthes 12.5MM REAMER HEAD FOR RIA 2 STERILE -Orthopedic manual surgical instrument Part Code: 03.404.021S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0582-2021·2020-12-23

    DePuy Synthes 15.5mm Reamer Head Recalled for Breakage and Tissue Damage

    Synthes (USA) Products LLC is recalling DePuy Synthes 15.5mm Reamer Heads for RIA 2 due to breakage exceeding expected rates, which can cause tissue and bone damage.

    Product
    DePuy Synthes 15.5MM REAMER HEAD FOR RIA 2 STERILE-Orthopedic manual surgical instrument Part Code: 03.404.027S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0573-2021·2020-12-23

    DePuy Synthes 11.0mm Reamer Head Recalled for Breakage and Tissue Damage

    Synthes (USA) Products LLC is recalling DePuy Synthes 11.0mm Reamer Heads for RIA 2 due to breakage exceeding expected rates, which can cause tissue and bone damage.

    Product
    DePuy Synthes 11.0MM REAMER HEAD FOR RIA 2 STERILE-Orthopedic manual surgical instrument Part Code: 03.404.018S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0581-2021·2020-12-23

    DePuy Synthes 15.0mm Reamer Head Recalled for Breakage and Tissue Damage

    Synthes (USA) Products LLC is recalling DePuy Synthes 15.0mm Reamer Heads for RIA 2 due to breakage rates exceeding expectations, which can cause tissue or bone damage.

    Product
    DePuy Synthes 15.0MM REAMER HEAD FOR RIA 2 STERILE -Orthopedic manual surgical instrument Part Code: 03.404.026S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0142-2021·2020-12-23

    High Dose B12 Injection Recalled for Sterility Assurance Concerns

    Advanced Nutriceuticals is recalling High Dose B12 vials because production processes cannot assure sterility. The product was distributed in seven states.

    Product
    HIGH DOSE B12, 10 MG/ML, 10 ML vial, The Guyer Institute of Molecular Medicine, Indianapolis, IN
    Category
    Drug
    Distribution
    7 states
  • SevereFDA (Devices)·Z-0574-2021·2020-12-23

    DePuy Synthes 11.5mm Reamer Head Recalled for Breakage Risk

    Synthes (USA) Products LLC is recalling DePuy Synthes 11.5mm Reamer Heads for RIA 2 due to breakage exceeding expected rates, which can cause tissue or bone damage.

    Product
    DePuy Synthes 11.5MM REAMER HEAD FOR RIA 2 STERILE-Orthopedic manual surgical instrument Part Code: 03.404.019S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0149-2021·2020-12-23

    BASF Recalls Crospovidone Excipient Due to Theophylline Contamination

    BASF Corporation is recalling 4,560 kg of Kollidon CL-M Crospovidone excipient because it was found to be cross-contaminated with theophylline.

    Product
    Kollidon CL-M Crospovidone Ph.Eur.Type B, USP/NF, JP, micronized, packaged in 30 kg plastic drums, Manufacturer: BASF SE, Carl-Bosch-Strabe 38, 67056 Ludwigshafen, Germany, Co-Manufactured by Siegfried PharmaChemikalien Minden GmbH, D-32423 Minden
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0140-2021·2020-12-23

    FDA Recalls Thymosin Beta-4 Vials Due to Sterility Concerns

    Advanced Nutriceuticals, LLC is recalling Thymosin Beta-4 vials because production processes cannot assure sterility. The product was distributed in seven states.

    Product
    THYMOSIN BETA - 4, 2000 MCG/ML, 5 ML vial, The Guyer Institute of Molecular Medicine, Indianapolis, IN
    Category
    Drug
    Distribution
    7 states
  • SevereFDA (Devices)·Z-0571-2021·2020-12-23

    DePuy Synthes 10.0MM Reamer Head Recalled for Breakage and Tissue Damage

    Synthes (USA) Products LLC is recalling DePuy Synthes 10.0MM Reamer Heads for RIA 2 because breakage exceeds expected rates, causing potential tissue or bone damage.

    Product
    DePuy Synthes 10.0MM REAMER HEAD FOR RIA 2, STERILE-Orthopedic manual surgical instrument Part Code: 03.404.016S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V808000·2020-12-22

    GM Recalls 2020 Chevrolet Bolt EV for Brake Caliper Fracture Risk

    General Motors is recalling 2020 Chevrolet Bolt EV vehicles because a front left brake caliper may fracture, potentially reducing brake performance and increasing crash risk.

    Product
    CHEVROLET — CHEVROLET BOLT EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V804000·2020-12-21

    Thor Motor Coach Recalls 2018-2019 Hurricane and Windsport Motorhomes

    Thor Motor Coach is recalling 2018-2019 Hurricane and Windsport motorhomes because overhead cabinets may detach and fall on occupants.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH HURRICANE, WINDSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V764000·2020-12-21

    GM Recalls 2010-2013 Buick and Chevrolet Models for Rear Suspension Defect

    General Motors is recalling specific Buick and Chevrolet vehicles because excessive corrosion protection on rear toe links may cause them to fracture, increasing crash risk.

    Product
    BUICK — BUICK, CHEVROLET LACROSSE, REGAL, MALIBU
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V802000·2020-12-21

    Mercedes-Benz and Freightliner Sprinter Vehicles Recalled for Brake Fluid Leak

    Daimler Vans USA is recalling 2019-2020 Mercedes-Benz and Freightliner Sprinter vans because rear brake calipers may leak fluid, allowing air into the hydraulic brake system.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, FREIGHTLINER SPRINTER 3500, SPRINTER 2500, SPRINTER 4500, SPRINTER 1500
    Category
    Vehicle
    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
  • 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
  • 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·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·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