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 the agency’s own highest classification or reported deaths or serious injuries, 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.

Filters

Agency

Category

Minimum severity

Clear filters

31176–31200 of 39756

  • CriticalFDA (Drugs)·D-1358-2014·2014-06-11

    Hospira Recalls Marcaine Injection Vials Due to Visible Metal Particles

    Hospira is recalling 85,680 vials of Marcaine (bupivacaine HCl) injection because a customer complaint confirmed the presence of visible metal particles and discolored solution.

    Product
    MARCAINE — MARCAINE (BUPIVACAINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2006-2014·2014-06-11

    Ste Fromagere du Livradois Recalls Raclette and Montboissie Cheeses for Salmonella Risk

    Ste Fromagere du Livradois is recalling specific lots of Raclette and Montboissie cheeses due to potential Salmonella contamination.

    Product
    Montboissie du haut- Livradois Manufactured by Ste Fromagere du Livradois 63980 Fournols 13lbs or cut and wrapped (weight may vary) wrapped in a wax paper in a case or wrapped in plastic wrap if cut; refrigerated
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Food)·F-2004-2014·2014-06-11

    Dragonfly Crushed Chili Powder Recalled for Salmonella Contamination

    U.S. Trading Co. is recalling Dragonfly Brand Crushed Chili Powder because an FDA sample tested positive for Salmonella B. reilly.

    Product
    Dragonfly Brand Crushed Chili Powder, Net Wt. 6.3 oz plastic tubs. Product of Thailand UPC 7 21557-53317 8 Packed for: U.S. Trading Co., 21118 Cabot Blvd., Hayward, CA 94545
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Drugs)·D-1357-2014·2014-06-11

    Losartan Potassium Tablets Recalled for Presence of Foreign Substance Debris

    Golden State Medical Supply Inc. is recalling Losartan Potassium 50 mg tablets because some bottles may contain debris swept up during cleaning.

    Product
    LOSARTAN POTASSIUM Tablets, USP, 50 mg, 30 count bottles, Rx only, Manufactured by Arrow Pharm (Malta) Ltd., Bizebbugia, Malta, Packaged by GSMS, Inc. Camarillo, CA --- NDC 60429-317-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1715-2014·2014-06-11

    Stryker NAV3i Platform Power Boxes Recalled for Missing Electrical Insulation

    Stryker is recalling 20 NAV3i Platform Power Boxes because they may lack electrical insulation on soldering joints, posing a shock hazard.

    Product
    The Stryker NAV3i Platform is a mobile cart platform consisting of the sub-components Stryker Nav3 Graphite Camera, SPC-3 Computer and IO-Tablet (touch screen) as well as the monitor, articulated arms and cart housing. This Navigation system is used in combination with surgical…
    Category
    Medical Device
    Distribution
    10 states
  • SevereFDA (Devices)·Z-1706-2014·2014-06-11

    GE Healthcare Recalls Kenex Ceiling Suspended Radiation Shields and Lamps

    GE Healthcare is recalling Kenex ceiling suspended radiation shields and surgical lamps due to improper installation. A reported incident involved a shield falling from the ceiling.

    Product
    Kenex Radiation Shield and surgical lamps installed with GE Healthcare Interventional, Surgery, CT and X-Ray Imaging systems. Kenex Suspension installed with Radiation shield and lamp with following model numbers…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1719-2014·2014-06-11

    ConMed Recalls MACROLYTE Premie Dispersive Electrodes Due to Sparking and Burning

    ConMed Corporation is recalling MACROLYTE Premie Dispersive Electrodes due to confirmed complaints of sparking, no output, and burning at the cord set connection.

    Product
    MACROLYTE Premie Dispersive Electrode, REF 440-2400, CONMED CORPORATION. The device is applied to the patient during electrosurgical procedures to provide a path for RF current to leave the patient and return to the generator.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1714-2014·2014-06-11

    Toshiba Infinix X-Ray System Recalled for Table Movement Safety Issue

    Toshiba is recalling two Infinix X-Ray Interventional Systems because the table may continue moving during longitudinal tilt despite error signals.

    Product
    Toshiba Infinix X-Ray Interventional System INFX-8000V/UU. An X-Ray system that is capable of radiographic and fluoroscopic studies used in an interventional setting.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V311000·2014-06-10

    Subaru Recalls Vehicles for Brake Line Corrosion Risk

    Subaru is recalling specific 2005-2014 models due to brake line corrosion from salt water, which may cause fluid leaks and increased stopping distances.

    Product
    SUBARU — SUBARU WRX STI, LEGACY, OUTBACK, IMPREZA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V310000·2014-06-10

    Hyundai Recalls Elantra Touring Vehicles Due to Headliner Bracket Hazard

    Hyundai is recalling 2010-2012 Elantra Touring vehicles because a headliner support bracket may become displaced during airbag deployment, posing a laceration risk.

    Product
    HYUNDAI — HYUNDAI ELANTRA TOURING
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V379000·2014-06-10

    UTEC Aerial Trucks Recalled for Potential Exhaust Fire Risk

    Utility Truck Equipment Company is recalling certain 2010-2013 UTEC aerial trucks and Ford chassis due to a PTO oil leak that could ignite the exhaust thermal blanket.

    Product
    UTEC — UTEC, FORD UTLN46, UTLI41A, F-550 SD, F-350 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V299000·2014-06-06

    GM Recalls 2014 Chevrolet Corvettes for Airbag Deactivation Risk

    General Motors is recalling 2014 Chevrolet Corvettes because a module short circuit may disable airbags and seat belt pretensioners.

    Product
    CHEVROLET — CHEVROLET CORVETTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V337000·2014-06-06

    Micro Bird Recalls G5 School Buses Due to Propane Leak Risk

    Micro Bird is recalling 2011-2013 G5 school buses with Roush propane systems because a metal reaction may cause a fuel leak, increasing fire risk.

    Product
    MICRO BIRD — MICRO BIRD G5 SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V300000·2014-06-06

    GM Recalls 2012 Vehicles for Driver Air Bag Deployment Failure

    General Motors is recalling specific 2012 Buick Verano, Chevrolet Cruze, Sonic, and Camaro vehicles because the driver's air bag may fail to deploy in a crash.

    Product
    CHEVROLET — CHEVROLET, BUICK CRUZE, SONIC, CAMARO, VERANO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V305000·2014-06-05

    KTM Recalls 2014 690 Enduro R Motorcycles Due to Rear Brake Pedal Defect

    KTM is recalling 649 model year 2014 690 Enduro R motorcycles because the rear brake pedal mounting bolt may loosen, allowing the pedal to detach and increasing crash risk.

    Product
    KTM — KTM 690 ENDURO R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1969-2014·2014-06-04

    Miravalle Ground Annato Spice Recalled for Potential Salmonella Contamination

    Miravalle Foods is recalling 0.75oz bottles of Achiote Molido Ground Annato spice due to potential Salmonella contamination. The product was distributed in seven western states.

    Product
    Miravalle (brand) Achiote Molido Ground Annato (spice), 0.75oz.
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Food)·F-1970-2014·2014-06-04

    Organic Traditions Dark Chocolate Recalled for Undeclared Milk Allergen

    Health Matters America Inc. is recalling Organic Traditions Dark Chocolate Golden Berries because the product contains undeclared milk, a major food allergen.

    Product
    Organic traditions DARK CHOCOLATE GOLDEN BERRIES***DAIRY & SUGAR FREE 80% DARK CHOCOLATE; Pack sizes 3.5oz/100g, UPC 8 54260 00263 8; 5.3 oz (150g), UPC 8 54260 00266 9; 12kg bulk boxes.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1972-2014·2014-06-04

    Price Chopper Tuscan White Bean Hummus Recalled for Undeclared Milk

    Golub Corporation is recalling Price Chopper brand Tuscan White Bean Hummus due to a labeling mix-up that resulted in an undeclared milk allergen.

    Product
    Price Chopper brand Hummus TUSCAN WHITE BEAN, NET WT. 10 OZ. Labels applied to clear plastic container with black rim on lid.
    Category
    Food
    Distribution
    6 states