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.

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31051–31075 of 39756

  • SevereFDA (Drugs)·D-1407-2014·2014-07-02

    Caraco Recalls Gemcitabine Injection Due to Sterility Assurance Concerns

    Caraco Pharmaceutical Laboratories is recalling 200 vials of Gemcitabine For Injection USP due to a lack of assurance of sterility.

    Product
    Gemcitabine For Injection USP, 1 g, (lyophilized), For Intravenous Use Only, Sterile Single Use Vial, Rx only, Manufactured by: Sun Pharmaceutical Ind. Ltd, Gujarat, India, NDC 47335-154-40
    Category
    Drug
    Distribution
    1 state
  • SevereNHTSA·14V405000·2014-07-02

    Ford Recalls 2014 F-53 and F-59 Chassis for Brake Caliper Defect

    Ford is recalling 2014 F-53 and F-59 chassis because incorrectly machined brake calipers may leak fluid, increasing stopping distances and crash risk.

    Product
    FORD — FORD F-59, F-53
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1823-2014·2014-07-02

    FDA Recalls HydroFinity Hydrophilic Guidewires Due to Jacket Damage

    Nitinol Devices and Components is recalling HydroFinity Hydrophilic Guidewires because the outer polymer jacket may be damaged during use.

    Product
    HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating, Sterile. 0.035 OD, Stiff Shaft, Straight Tip, 260 CM Length; Manufactured for Covidien, Plymouth, MN; Manufactured by: NDC Inc., Fremont, CA; Manufactured in Costa Rica The HydroFinity…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1815-2014·2014-07-02

    Nitinol Devices Recalls HydroFinity Hydrophilic Guidewires Due to Jacket Damage

    Nitinol Devices and Components, Inc. is recalling HydroFinity Hydrophilic Guidewires because the outer polymer jacket may be damaged during use.

    Product
    HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating, Sterile. 0.035 OD, Standard Shaft, Straight Tip, 150 CM Length Manufactured for Covidien, Plymouth, MN; Manufactured by: NDC Inc., Fremont, CA. Manufactured in Costa Rica The HydroFinity…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1819-2014·2014-07-02

    Nitinol HydroFinity Hydrophilic Guidewire Recalled for Polymer Jacket Damage

    Nitinol Devices and Components, Inc. is recalling HydroFinity Hydrophilic guidewires because reports indicate the outer polymer jacket may be damaged during use.

    Product
    HydroFinity Hydrophilic guidewire;Nitinol Guidewire with Hydrophilic Coating, Sterile. 0.035 OD, Stiff Shaft, Angled Tip, 180 CM Length; Manufactured for Covidien, Plymouth, MN; Manufactured by: NDC Inc., Fremont, CA Manufactured in Costa Rica. The HydroFinity…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V398000·2014-07-02

    Fontaine Recalls 2015 Magnitude 100 Trailers Due to Weld Defects

    Fontaine is recalling 2015 Magnitude 100 lowbed trailers because inadequate welds may cause structural components to separate, increasing crash risk.

    Product
    FONTAINE — FONTAINE MAGNITUDE 100
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2051-2014·2014-07-02

    Eillien's Dark Old Fashioned Sponge Candy Recalled for Undeclared Milk

    Eillien's Candies is recalling Dark Old Fashioned Sponge Candy because it contains undeclared milk, posing a risk to consumers with milk allergies.

    Product
    Dark Old Fashioned Sponge Candy, sold under the following brand and sizes: 1. Eillien's in Net Wt. 6 oz (170g) UPC 34952-12994, 10 oz. (284g) UPC 34952-56927, 12 oz. (340g) UPC 34952-57307. 2. Blain's Farm & Fleet Net Wt. 14oz. (397g), UPC 34952-81171 3. Mae's Corner…
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Devices)·Z-1812-2014·2014-07-02

    FDA Recalls HydroFinity Hydrophilic Guidewires Due to Polymer Jacket Damage

    Nitinol Devices and Components is recalling HydroFinity Hydrophilic Guidewires because the outer polymer jacket may be damaged during use.

    Product
    HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating, Sterile. 0.035 OD, Standard Shaft, Angled Tip, 150 CM Length Manufactured for Covidien, Plymouth, MN; Manufactured by: NDC Inc., Fremont, CA. Manufactured in Costa Rica The HydroFinity…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V407000·2014-07-02

    GM Recalls 2007-2011 Silverado and Sierra Trucks for Fire Risk

    General Motors is recalling 2007-2011 Chevrolet Silverado and GMC Sierra HD trucks equipped with auxiliary batteries due to a risk of electrical fire.

    Product
    GMC — GMC, CHEVROLET SIERRA 3500, SIERRA 2500, SILVERADO 2500, SILVERADO 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1818-2014·2014-07-02

    Nitinol Recalls HydroFinity Hydrophilic Guidewires Due to Jacket Damage

    Nitinol Devices and Components is recalling HydroFinity Hydrophilic Guidewires because reports indicate the outer polymer jacket can be damaged during use.

    Product
    HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating, Sterile. 0.035 OD, Stiff Shaft, Angled Tip, 150 CM Length; Manufactured for Covidien, Plymouth, MN; Manufactured by: NDC Inc., Fremont, CA Manufactured in Costa Rica The HydroFinity…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1813-2014·2014-07-02

    Nitinol HydroFinity Hydrophilic Guidewire Recalled for Outer Polymer Jacket Damage

    Nitinol Devices and Components is recalling HydroFinity Hydrophilic Guidewires because the outer polymer jacket may be damaged during use.

    Product
    HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating, Sterile. 0.035 OD, Standard Shaft, Angled Tip, 180 CM Length; Manufactured for Covidien, Plymouth, MN; Manufactured by: NDC Inc., Fremont, CA. Manufactured in Costa Rica The HydroFinity…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2030-2014·2014-07-02

    Key Lime Dip Recalled for Undeclared Allergens in Compound Ingredients

    Miami Interculinary Center, Inc. is recalling 1,164 bottles of Floribbean Key Lime Calypso Dip because the label failed to declare allergens in compound ingredients.

    Product
    Floribbean Key Lime Calypso Dip 12.5 oz Floribbean 68 SW 40 St. Suite 411 Miami, Florida 33155 1(800)282-8459
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Drugs)·D-1408-2014·2014-07-02

    Teva Recalls Dextroamphetamine Sulfate Tablets Due to Impurity Test Failures

    Teva Pharmaceuticals is recalling 9,882 bottles of Dextroamphetamine Sulfate 10 mg tablets because stability testing revealed out-of-specification impurities.

    Product
    DEXTROAMPHETAMINE SULFATE — DEXTROAMPHETAMINE SULFATE (DEXTROAMPHETAMINE SULFATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1821-2014·2014-07-02

    Nitinol HydroFinity Hydrophilic Guidewire Recalled for Outer Polymer Jacket Damage

    Nitinol Devices and Components, Inc. is recalling HydroFinity Hydrophilic guidewires because the outer polymer jacket may be damaged during use.

    Product
    HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating, Sterile. 0.035 OD, Stiff Shaft, Straight Tip, 150 CM Length; Manufactured for Covidien, Plymouth, MN; Manufactured by: NDC Inc., Fremont, CA. Manufactured in Costa Rica The HydroFinity…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1814-2014·2014-07-02

    Nitinol HydroFinity Hydrophilic Guidewire Recalled for Outer Polymer Jacket Damage

    Nitinol Devices and Components is recalling HydroFinity Hydrophilic guidewires because reports indicate the outer polymer jacket may be damaged during use.

    Product
    HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating, Sterile. 0.035 OD, Standard Shaft, Angled Tip, 260 CM Length; Manufactured for Covidien, Plymouth, MN; Manufactured by: NDC Inc., Fremont, CA. Manufactured in Costa Rica The HydroFinity…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V402000·2014-07-02

    Ford Recalls 2014 Fiesta Vehicles Due to Fuel Tank Leak Risk

    Ford is recalling certain 2014 Fiesta vehicles because a manufacturing error may cause the fuel tank to leak, increasing the risk of fire.

    Product
    FORD — FORD FIESTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V397000·2014-07-02

    Autocar Recalls 2012-2015 Xpert Trucks Due to Bounce Hazard

    Autocar is recalling 287 model year 2012-2015 Xpert trucks because a gap between the cab and body may cause unexpected bouncing at speeds above 25 mph, increasing crash risk.

    Product
    AUTOCAR — AUTOCAR XPERT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V403000·2014-07-02

    Ford Recalls 2014 Escape Vehicles for Panorama Roof Glass Bonding Defect

    Ford is recalling 2014 Escape vehicles because the panorama roof glass may not be properly bonded, which could cause the glass to separate and increase the risk of a crash or injury.

    Product
    FORD — FORD ESCAPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14E034000·2014-07-02

    LiquidSpring Recalls Aftermarket Suspensions for Ford and Chevrolet Chassis

    LiquidSpring is recalling specific aftermarket suspension units for Ford and Chevrolet chassis because a mounting bracket may fail, allowing the fluid tank to separate and become a road hazard.

    Product
    SUSPENSION recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V393000·2014-07-02

    Ford and Lincoln Recall Vehicles for Halfshaft Retention Defect

    Ford is recalling 2012-2014 Edge, MKX, Taurus, MKS, Flex, and MKT vehicles because a halfshaft may disengage, causing loss of power or vehicle roll-away.

    Product
    LINCOLN — LINCOLN, FORD MKS, FLEX, EDGE, TAURUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1854-2014·2014-07-02

    NxStage Dialysate Sacks Recalled for Excess Aluminum Levels

    NxStage Medical is recalling dialysate sacks used with the PureFlow SL system because they contain aluminum levels exceeding internal specifications.

    Product
    NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow SL REF: SAK-301 Lactate 45, Potassium 1, Sodium 140, Calcium 3, Magnesium 1, Chloride 100, Glucose (mg/dL) 100 Batch Size (liters) 60 The SAK is one of the disposables used with NxStage PureFlow SL…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1925-2014·2014-07-02

    Biomet Recalls Discovery Elbow Prosthesis Due to Surface Finish Defect

    Biomet, Inc. is recalling one unit of a Discovery Elbow prosthesis because the surface finish differs from specifications, potentially causing pain requiring surgery.

    Product
    DISCOVERY ELBOW prosthesis, 4 MM X 100 MM RIGHT HUMERAL FLANGED I BOND COAT Tl 6AL 4V ALLOY. Elbow joint replacement prostheses are intended for primary and revision joint arthroplasty for use in cemented applications.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V409000·2014-07-02

    GM Recalls 2014 Vehicles for Steering Component Separation Risk

    General Motors is recalling 2014 Buick Regal, Cadillac XTS, Chevrolet Camaro, and Chevrolet Impala vehicles because improperly torqued fasteners may cause steering components to separate, increasing crash risk.

    Product
    CHEVROLET — CHEVROLET, BUICK, CADILLAC IMPALA, CAMARO, REGAL, XTS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V401000·2014-07-02

    Ford Recalls F-59 Commercial Chassis Vehicles for Fire Risk

    Ford is recalling 2011-2014 F-59 commercial chassis vehicles because a short circuit in the electrical system may cause a fire.

    Product
    FORD — FORD F-59
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V392000·2014-07-02

    Chrysler Recalls 2014-2015 Vehicles for Rear Shock Absorber Weld Defect

    Chrysler is recalling 2014 Jeep Cherokee, Ram 1500, and 2015 Chrysler 200 vehicles because an insufficient weld may cause rear shocks to detach, potentially damaging tires or reducing braking.

    Product
    CHRYSLER — CHRYSLER, RAM, JEEP 200, 1500, CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide