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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34501–34525 of 39756

  • SevereFDA (Food)·F-1554-2013·2013-07-03

    Bimbo Bakeries Recalls Earthgrains Hot Dog Buns Due to Metal Fragments

    Bimbo Bakeries USA is recalling 8,572 units of Earthgrains Hot Dog Buns due to possible metal fragments caused by a faulty manufacturing part.

    Product
    Hot Dog Buns 8 Count Earthgrains Baking companies, Inc. Horsham, PA 19044
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-1573-2013·2013-07-03

    Medtronic Sutureless Pump Connector Revision Kit Recalled for Occlusion Risk

    Medtronic is recalling Sutureless Pump Connector Revision Kits due to a design flaw that increases the risk of catheter occlusion.

    Product
    Medtronic Sutureless Pump Connector Revision Kit, model 8578. Contents: catheter interface with attached sutureless pump connector, catheter, connector pin, and strain-relief sleeve to be used with Medtronic SynchroMed implantable drug infusion pumps. Contents of inner…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-614-2013·2013-07-03

    Hospira Recalls 5% Dextrose Injection Due to Sterility Concerns

    Hospira is voluntarily recalling 5% Dextrose Injection USP bags due to possible leaking that compromises sterility assurance.

    Product
    5% Dextrose Injection USP, a) 250 mL (NDC 0409-7922-02), b) 500 mL (NDC 0409-7922-30), by Hospira, Inc., Lake Forest, IL 60045
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V288000·2013-07-02

    Chrysler Recalls 2013 RAM Trucks Due to Track Bar Bolt Defect

    Chrysler is recalling 2013 RAM 4500 and 5500 trucks because an incorrect bolt may break, causing the vehicle to pull to one side and increasing crash risk.

    Product
    RAM — RAM 5500, 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V291000·2013-07-02

    Chrysler Recalls 2013 Minivans Due to Air Bag Software Defect

    Chrysler is recalling 2013 Town & Country and Dodge Grand Caravan minivans because incorrect software in the occupant restraint control module may affect air bag deployment.

    Product
    DODGE — DODGE, CHRYSLER GRAND CARAVAN, TOWN AND COUNTRY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V282000·2013-07-02

    Chrysler Recalls 2011-2013 Vehicles for Active Head Restraint Defect

    Chrysler is recalling specific 2011-2013 models because electrical issues may prevent active head restraints from deploying in rear-end collisions, increasing injury risk.

    Product
    DODGE — DODGE, JEEP, CHRYSLER AVENGER, LIBERTY, 200, SEBRING
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V284000·2013-07-01

    Monaco RV Recalls 2,250 Vehicles Due to Water Tank Mounting Failure

    Monaco RV is recalling 2,250 recreational vehicles because the water tank mounting system may fail, causing the tank to separate and become a road hazard.

    Product
    R-VISION — R-VISION, MCKENZIE, HOLIDAY RAMBLER TRAIL SPORT, ONYX, RAINIER ASCENT, ALUMA-LITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V276000·2013-06-28

    Altec Lift-All LSS Aerial Devices Recalled for Turntable Cracks

    Altec is recalling 2008-2009 Lift-All LSS aerial devices because cracks in the turntable may cause failure, increasing the risk of personal injury.

    Product
    ALTEC LLC — ALTEC LLC LIFT-ALL LSS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V271000·2013-06-27

    GM Recalls 2012 Chevrolet Volt for Brake Pressure Valve Defect

    General Motors is recalling specific 2012 Chevrolet Volt vehicles because a brake pressure modulator valve issue may cause front brakes to lock up during safety system events.

    Product
    CHEVROLET — CHEVROLET VOLT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V281000·2013-06-27

    La Boit Recalls 2013 Mobile Services Vehicles Due to Awning Motor Defect

    La Boit is recalling 2013 Mobile Services vehicles because power awning motor screws may shear, causing the awning to unfurl unexpectedly and increasing crash risk.

    Product
    LA BOIT — LA BOIT MOBILE SERVICES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V274000·2013-06-27

    Amerivan Toyota Sienna Vans Recalled for Fuel Filler Neck Contact

    Eldorado National is recalling 2011-2013 Amerivan Toyota Sienna vans because the fuel filler neck may contact the shock absorber, risking a fire.

    Product
    AMERIVAN — AMERIVAN TOYOTA SIENNA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1547-2013·2013-06-26

    Vega One Nutrition Bar Recalled for Unlabeled Milk Ingredients

    Sequel Naturals Ltd is recalling Vega One Double Chocolate nutrition bars because milk ingredients were inadvertently added to the chocolate coating, posing a risk to consumers with milk allergies.

    Product
    vega one, all-in one nutrition bar; Double chocolate flavor Added vitamins and minerals; 15 g Protein, 6 g Fiber and 1.5 g Omega Antioxidants, probiotics & greens; Gluten Free Dietary Supplement. 2.2 oz/ 63g Made in a facility that processes peanuts, tree nuts, sesame…
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1548-2013·2013-06-26

    Vega Sport Chocolate Coconut Protein Bar Recalled for Unlabeled Milk

    Sequel Naturals Ltd is recalling Vega Sport Chocolate Coconut protein bars because milk ingredients were inadvertently added to the chocolate coating. One allergic reaction has been reported.

    Product
    vega sport, Natural Plant-Based Protein Bar; Chocolate Coconut flavor Gluten Free; 2.1 oz/ 60g Complete protein " 4g of fiber per serving " 0.4g of Omega-3 per serving Made in a facility that processes peanuts, tree nuts, sesame, dairy, and soy. May contain fruit shell or…
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1549-2013·2013-06-26

    Vega Sport Protein Bar Recalled for Unlabeled Milk Ingredients

    Sequel Naturals Ltd is recalling Vega Sport Natural Plant-Based Protein Bars because milk ingredients were inadvertently added to the chocolate coating, posing a risk to consumers with milk allergies.

    Product
    vega sport, Natural Plant-Based Protein Bar; Chocolate Saviseed flavor Gluten Free; 2.1 oz/ 60g Complete protein " 4g of fiber per serving " 0.4g of Omega-3 per serving Made in a facility that processes peanuts, tree nuts, sesame, dairy, and soy. May contain fruit shell or…
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1545-2013·2013-06-26

    Vega One Nutrition Bar Recalled for Unlabeled Milk Ingredients

    Sequel Naturals Ltd is recalling Vega One chocolate almond nutrition bars because milk ingredients were inadvertently added to the chocolate coating, posing a risk to consumers with milk allergies.

    Product
    vega one, all-in one nutrition bar; chocolate almond flavor Added vitamins and minerals; 15 g Protein, 6 g Fiber and 1.5 g Omega Antioxidants, probiotics & greens; Gluten Free Dietary Supplement. 2.2 oz/ 63g Made in a facility that processes peanuts, tree nuts, sesame…
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1546-2013·2013-06-26

    Vega One Nutrition Bar Recalled for Unintended Milk Ingredients

    Sequel Naturals Ltd is recalling Vega One chocolate cherry nutrition bars because milk ingredients were inadvertently added to the chocolate coating.

    Product
    vega one, all-in one nutrition bar; chocolate cherry flavor Added vitamins and minerals; 15 g Protein, 6 g Fiber and 1.5 g Omega Antioxidants, probiotics & greens; Gluten Free Dietary Supplement. 2.2 oz/ 63g Made in a facility that processes peanuts, tree nuts, sesame…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1558-2013·2013-06-26

    Verathon Recalls GlideScope Reusable Laryngoscope Blades Due to Breakage Risk

    Verathon is recalling GlideScope reusable laryngoscope blades because the tips may break prematurely without visible signs, posing a risk to patients during intubation.

    Product
    GlideScope Video Laryngoscope (GVL) 3, 4, 5 and GlideScope (AVL) 2, 3, 4 and 5 reusable blades Product Usage: The GlideScope Video Laryngoscopes are intended for use by qualified medical professionals to obtain a clear, unobstructed view of the vocal cords for medical…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-609-2013·2013-06-26

    Pharmacia Recalls Cleocin Phosphate Vials Due to Glass Delamination

    Pharmacia & Upjohn LLC is recalling specific lots of Cleocin Phosphate injection vials due to the presence of very small reflective flakes consistent with glass delamination.

    Product
    CLEOCIN PHOSPHATE — CLEOCIN PHOSPHATE (CLINDAMYCIN PHOSPHATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V268000·2013-06-26

    Volvo Trucks Recall 2007-2014 Models Due to Clutch Disengagement Defect

    Volvo is recalling 23,056 heavy-duty trucks from 2007-2014 because a missing redundant switch may prevent the clutch from disengaging, increasing stopping distance.

    Product
    VOLVO — VOLVO VNL, VNM, VT, VAH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1533-2013·2013-06-26

    Lightlife Veggie Burgers Recalled for Undeclared Milk Allergen

    Conagra is recalling Lightlife Farmer's Market Veggie Burgers because packaging may contain milk-containing products, and the milk allergen is not declared on the label.

    Product
    Lightlife Farmer's Market Veggie Burgers, meat free, 12 oz/4-count bag, packaged in 5/12 oz-bag/cartons. Distributed By: Lightlife Foods, Turners Falls, MA. Case UPC Code: 20043454805252
    Category
    Food
    Distribution
    33 states
  • SevereFDA (Drugs)·D-606-2013·2013-06-26

    Teva Recalls Actiq Fentanyl Lozenges Due to Dissolution Failure

    Teva Pharmaceuticals is recalling 316 cartons of Actiq 200 mcg fentanyl lozenges because they failed dissolution specifications during stability testing.

    Product
    Actiq (oral transmucosal fentanyl citrate) 200 mcg, lozenge on a stick, a)Single Blister (NDC 63459-502-01), b) 30 count carton (NDC 63459-502-30), Rx only, Manufactured by: Cephalon, Inc., Salt Lake City, UT 84116
    Category
    Drug
    Distribution
    7 states
  • SevereFDA (Drugs)·D-605-2013·2013-06-26

    Sagent Recalls Vecuronium Bromide Injection Due to Manufacturing Deviations

    Sagent Pharmaceuticals is recalling Vecuronium Bromide for Injection because it was not manufactured under current good manufacturing practices, resulting in failed impurity specifications.

    Product
    VECURONIUM Bromide for Injection, 10 mg* per vial, *1 mg per mL when reconstituted to 10 mL, for IV single use only, Rx only, Mfd. for SAGENT Pharmaceuticals, Schaumburg, IL 60195 (USA); Mfd. by MN Pharmaceuticals; Made in Turkey, NDC 25021-657-10.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1537-2013·2013-06-26

    Respironics V60 Ventilator Recalled for Power Management Board Software Issue

    Respironics is recalling V60 ventilators due to a software issue on the Power Management Board Assembly that could cause loss of ventilator support without an audible alarm.

    Product
    Respironics V60 Ventilator, Model #V60 Respironics Material P/N (Philips 12 Digit P/N): 85008 (85008) 1053613 (989805628251) 1053614 (989805612101) 1053615 (989805613391) 1053616 (989805613661) 1053617 (989805611761) 1053618 (n/a) R1053618 (n/a) 1076709 (n/a)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1548-2013·2013-06-26

    Biomet Recalls Superior Approach Resection Guide Assembly Due to Slot Offset

    Biomet is recalling 17 units of the Superior Approach Resection Guide Assembly because a manufacturing defect may prevent the guide from securing properly to bone during surgery.

    Product
    Superior Approach Resection Guide Assembly. Indicated for primary, fracture, or revision total shoulder replacement for the relief of pain.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1544-2013·2013-06-26

    Julian's Recipe Pretzel Baguette Recalled for Undeclared Soy Flour

    Julian's Recipe is recalling specific lots of European Style Pretzel Baguettes due to an undeclared soy flour ingredient caused by a repacking error.

    Product
    ALL NATURAL Julian's RECIPE European Style Pretzel Baguette, BUTTER & SEA SALT, NET WT 11.3 OZ (320 g), UPC 8 55971 00226 9, 2 BAGUETTES, KEEP FROZEN -- Product of Germany. Manufactured for Distribution by Julian's Recipe, LLC PO Box 323, Montgomery, NY 12549. --- The product…
    Category
    Food
    Distribution
    1 state