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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31551–31575 of 39756

  • SevereNHTSA·14V183000·2014-04-07

    Oshkosh Recalls S-Series Trucks Due to Exhaust Fire Risk

    Oshkosh is recalling 2012-2014 S-Series Ready Mixed Concrete trucks because condensation in the intake manifold may freeze, causing elevated exhaust temperatures or flames that increase the risk of fire or burn injury.

    Product
    OSHKOSH — OSHKOSH S-SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V172000·2014-04-04

    MCI E4500 and J4500 Motorcoaches Recalled for Seat Track Weld Defect

    Motor Coach Industries is recalling 2009-2014 E4500 and J4500 motorcoaches because a missing weld on second-row seat tracks could cause seats to detach in a crash.

    Product
    MCI — MCI J4500, E4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·14144·2014-04-04

    Hussong Recalls Gas Fireplaces and Inserts Due to Explosion Hazard

    Hussong Manufacturing is recalling about 13,600 gas fireplaces and inserts in the U.S. because a control module defect can cause gas buildup and explosions.

    Product
    Kozy Heat, Ambiance and Stellar Hearth gas fireplaces and fireplace inserts
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V238000·2014-04-03

    Navistar Recalls 2014 International TranStar Trucks Due to Fire Risk

    Navistar is recalling 2014 International TranStar trucks with specific Cummins engines because condensation may freeze and cause exhaust flames or fire.

    Product
    INTERNATIONAL — INTERNATIONAL TRANSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V173000·2014-04-03

    Mazda Recalls 2014-2015 Models for Potential Engine Stall Risk

    Mazda is recalling 2014-2015 Mazda3 and Mazda6 vehicles because a software error may cause the engine to stall in heavy rain, increasing crash risk.

    Product
    MAZDA — MAZDA MAZDA6, MAZDA3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1227-2014·2014-04-02

    Thoratec HeartMate II Implant Kit Recalled Due to Controller Switching Injuries

    Thoratec is recalling HeartMate II Implant Kits because serious injuries and deaths occurred when patients switched from primary to backup System controllers.

    Product
    HeartMate II Implant Kit with Pocket Controller; with sealed grafts (NAm) with sealed grafts (EU) Product Usage: HeartMate II is a mechanical device that circulates blood throughout the body when the heart is too weak to pump blood adequately on its own.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1230-2014·2014-04-02

    Thoratec HeartMate II Pocket Controllers Recalled Due to Reported Deaths

    Thoratec is recalling HeartMate II Pocket Controllers because serious injuries and deaths were reported when patients switched from primary to backup controllers.

    Product
    Heart Mate II Pocket Controllers removed from packaging Product Usage: HeartMate II is a mechanical device that circulates blood throughout the body when the heart is too weak to pump blood adequately on its own.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1228-2014·2014-04-02

    Thoratec HeartMate II System Controller Recalled Due to Injury and Death Reports

    Thoratec is recalling HeartMate II System Controllers because serious injuries and deaths occurred when patients switched from primary to backup controllers.

    Product
    HeartMate II System Controller Product Usage: HeartMate II is a mechanical device that circulates blood throughout the body when the heart is too weak to pump blood adequately on its own. It is sometimes called a a heart pump or VAD. HeartMate II is a small implantable LVAD.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1696-2014·2014-04-02

    Kinnikinnick Panko Bread Crumbs Recalled for Undeclared Milk

    World Pure Foods Wholesalers is recalling Kinnikinnick Panko Style Bread Crumbs sold in Michigan due to undeclared milk.

    Product
    Kinnikinnick Panko Style Bread Crumbs-Weight: 350g/12.5oz Cardboard Box UPC 62013360015 3
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-1694-2014·2014-04-02

    Kinnikinnick Waffles Recalled for Undeclared Milk Allergen

    World Pure Foods Wholesalers is recalling Kinnikinnick Original Homestyle Waffles sold in Michigan due to undeclared milk.

    Product
    Kinnikinnick Original Homestyle Waffles 210 g/7.4 oz Cardboard Box UPC 620133001981
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Devices)·Z-229-2014·2014-04-02

    Thoratec HeartMate II LVAD Pump Recall Due to Controller Switching Injuries

    Thoratec is recalling 36 HeartMate II LVAD Pump and Pocket Controller Kits because switching from the primary to the backup controller caused serious injuries and deaths.

    Product
    HeartMate II LVAD Pump and Pock Controller Kit; Product Usage: HeartMate II is a mechanical device that circulates blood throughout the body when the heart is too weak to pump blood adequately on its own.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1702-2014·2014-04-02

    Dole Italian Blend Salad Recalled for Listeria Monocytogenes

    Dole Fresh Vegetables Inc is recalling Italian Blend Salad due to a positive Listeria Monocytogenes test by the Canadian Food Inspection Agency.

    Product
    Italian blend Salad (Romaine Lettuce and Radicchio) packaged under the following brand names: Dole Italian Blend, (UPC 7143000819); Fresh Selections Italian Style Blend (Kroger) (UPC 1111091045); Little Salad Bar Italian Salad, (UPC 4149811014); Marketside Italian Style…
    Category
    Food
    Distribution
    15 states
  • SevereFDA (Food)·F-1699-2014·2014-04-02

    Nutra Balance Pre-Thickened Water Recalled Due to Mold Contamination

    Nutra Balance Products is recalling 432 units of Thickened Water Pudding Thick Phase 3 because the product was found to contain mold.

    Product
    Thickened Water Pudding Thick 32 oz. (944ml) Phase 3 Ingredients: Pasteurized Filtered Water, Cellulose Gum Fibre, Potassium Sorbate.
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Food)·F-1695-2014·2014-04-02

    Kinnikinnick Waffles Recalled for Undeclared Milk Allergen

    World Pure Foods Wholesalers is recalling Kinnikinnick Cinnamon & Brown Sugar Homestyle Waffles sold in Michigan due to undeclared milk.

    Product
    Kinnikinnick Cinnamon & Brown Sugar Homestyle Waffles 210 g/7.4 oz Cardboard Box UPC 620133001981
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1689-2014·2014-04-02

    Jin Sun Mi Recalls Watermelon Ice Bars for Undeclared Peanuts

    Jin Sun Mi International is recalling watermelon ice bars because they contain undeclared peanuts.

    Product
    Frozen Ice Cake (Watermelon), 17.98 oz, 6 retail units/carton, UPC 8 801062 443055
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1301-2014·2014-04-02

    BioCardia Morph AccessPro Steerable Introducer Recalled for Particulate Risk

    BioCardia is recalling Morph AccessPro Steerable Introducers due to potential particulates in the inner lumen that could cause an embolic event.

    Product
    Morph AccessPro Steerable Introducer; 6F Introducer, 45 cm working length Single use only. BioCardia, Inc. San Carlos, CA 94070 BioCardia Morph AccessPro is intended to provide a pathway through medical instruments cush as balloon dilation catheters, guidewires or other…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1272-2014·2014-04-02

    Siemens AXIOM Artis Systems Recalled for Potential Gantry Drop Risk

    Siemens is recalling 37 AXIOM Artis angiography systems because a cooling unit defect may cause a system failure and gantry drop.

    Product
    AXIOM Artis Systems Product usage: Artis zee is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1700·2014-04-02

    Nutra Balance Thickened Water Recalled for Mold and Bacteria

    Nutra Balance Products is recalling Thickened Water Nectar Thick due to FDA findings of mold. A related product also tested positive for bacteria.

    Product
    Thickened Water Nectar Thick 32 oz. (944ml) Phase 1 Ingredients: Pasteurized Filtered Water, Cellulose Gum Fibre, Potassium Sorbate, Citric Acid.
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Devices)·Z-1275-2014·2014-04-02

    Velocity Medical Solutions Recalls DICOM Export Format Software

    Velocity Medical Solutions is recalling DICOM Export Format for Sum Dose v3.0.0 software because it may replace calculated doses in Eclipse treatment plans.

    Product
    DICOM Export Format for Sum Dose with Velocity v3.0.0. A stand-alone software product that provides the oncology care specialists (physicians, physicists, dosimetrists, etc.) a means for comparison of medical imaging data from multiple DICOM conformant imaging modality…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V164000·2014-04-02

    Ford Recalls 2013-2014 Vehicles Due to Weak Seatback Welds

    Ford is recalling 2013-2014 Fusion, Escape, C-Max, and Lincoln MKZ vehicles because sub-standard welds may cause seatbacks to loosen, increasing injury risk in crashes.

    Product
    FORD — FORD, LINCOLN ESCAPE, MKZ, C-MAX, FUSION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·020-2014·2014-04-02

    Backpackers Pantry Recalls Fettuccini Alfredo With Chicken Due to Undeclared Allergens

    American Outdoor Products is recalling 633 pounds of dehydrated Fettuccini Alfredo with Chicken because the packaging contains undeclared milk and wheat allergens.

    Product
    American Outdoor Products, Inc — Colorado Firm Recalls Fettuccini Alfredo With Chicken Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide