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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34901–34925 of 39756

  • SevereNHTSA·13V199000·2013-05-14

    Starcraft Allstar Buses Recalled for Wheelchair Lift Cable Fire Risk

    Starcraft is recalling 2006-2012 Allstar buses because a wheelchair lift cable may not clear the lift, potentially causing a short circuit and fire.

    Product
    STARCRAFT — STARCRAFT ALLSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V194000·2013-05-13

    Subaru Recalls 2013 Outback and Legacy for Steering Column Defect

    Subaru is recalling 2013 Outback and Legacy vehicles because the steering column shafts may disengage, causing loss of steering control.

    Product
    SUBARU — SUBARU OUTBACK, LEGACY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V196000·2013-05-13

    Maserati Recalls 2005-2008 Models for Rear Tie Rod Corrosion Risk

    Maserati is recalling 7,438 vehicles due to insufficient anti-corrosion material on rear tie rods, which may weaken and fail, increasing crash risk.

    Product
    MASERATI — MASERATI, ALFA ROMEO QUATTROPORTE, GRANTURISMO, 8C
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V191000·2013-05-13

    New Heights Recalls Equipter RB4000 Dump Trailers for Brake Defect

    New Heights LLC is recalling Equipter RB4000 dump trailers manufactured in December 2011 because a defective hydraulic brake actuator could cause a loss of braking ability.

    Product
    SERVICE BRAKES, HYDRAULIC recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·13189·2013-05-10

    Meijer Recalls Touch Point Baseboard Heaters Due to Fire Hazard

    Meijer is recalling Touch Point portable baseboard convection heaters because they can overheat and cause fires. Consumers should stop using the units and return them for a refund.

    Product
    Touch Point Portable Baseboard Convection Heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V187000·2013-05-09

    KME Emergency Vehicles Recalled for Steering Column Grease Fitting Defect

    Kovatch is recalling specific KME emergency vehicles because a grease fitting in the steering column may tear the cover, potentially causing a loss of steering control.

    Product
    KME — KME PREDATOR SS, ARFF, PREDATOR, PANTHER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V188000·2013-05-09

    Magic Tilt Boat Trailer Hydraulic Brake Actuator Recall

    Magic Tilt is recalling boat trailers with defective hydraulic brake actuators that may fail, causing loss of braking ability and increasing crash risk.

    Product
    SERVICE BRAKES, HYDRAULIC recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1371-2013·2013-05-08

    DZH Import Recalls Dried Mushrooms for Undeclared Sulfites

    DZH Import & Export Inc. is recalling two brands of dried mushrooms sold in New York City because they contain undeclared sulfites.

    Product
    Dried mushrooms sold under the following brand names: 1) CURIOSITY OF DASHAN brand DRIED MUSHROOM, N.W. 100G (3.5 OZ), UPC 6 939457 003484, Product of China --- Imported By: DZH Import & Export Inc. 70-21 51 Avenue, Woodside, NY 11377 Tel: 718-205-8312 Fax: 718-205-8146…
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-1369-2013·2013-05-08

    Farm Rich Pizza Dippers Recalled Due to E. coli O121 Contamination

    Rich Products Corp is recalling Farm Rich Better For You Pizza Dippers nationwide due to potential E. coli O121 contamination.

    Product
    Farm Rich Better For You Pizza Dippers-Pizza Dough made with Whole Wheat Flour and Stuffed with Mozzarella Cheese and Reduced Fat Mozzarella Cheese, Net Wt. 27-LBS (10 X 2.7-LB), UPC Code 00041322652782, Product Code 65278.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1170-2013·2013-05-08

    Hospira Recalls GemStar Infusion Pumps Due to Unexpected Shutdowns

    Hospira Inc. is recalling GemStar infusion pumps because they may shut off during use without warning, potentially interrupting patient medication delivery.

    Product
    The GemStar Pump is a small and lightweight, single channel infusion device designed for use in the home, in the hospital, or anywhere electronic infusion is required. The GemStar Pump can be powered by AC mains adaptor, rechargeable battery pack, docking station, or two…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1189-2013·2013-05-08

    Philips HeartStart MRx Monitor/Defibrillator Recalled for Therapy Failure Risk

    Philips is recalling HeartStart MRx Monitor/Defibrillators because they may fail to deliver defibrillation therapy in Manual Defib or AED mode.

    Product
    HeartStart MRx Monitor/Defribillator; Product Codes: M3536A, M3536J, M3536M, M3536MC, M3536M2, M3536M4, M3536M5, M3536M6. The HeartStart MRx is for use for the termination of ventricular tachycardia and ventricular fibrillation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1373-2013·2013-05-08

    Buffalo Trace Bourbon Fudge Sauce Recalled for Missing Allergen Labeling

    Buffalo Trace Distillery is recalling 1,686 jars of Bourbon Fudge Sauce because the label failed to list milk and soy allergens.

    Product
    BUFFALO TRACE BOURBON FUDGE SAUCE 8 oz glass jars Net Wt. 8 fl. oz./227 g, PRODUCED BY: APPLECREEK ORCHARDS LLC P.O. Box 8383 Lexington, KY 40533 BUFFALO TRACE DISTILLERY 113 Great Buffalo Trace Franklin County Frankfort, KY 40601 800-654-8471 e-mail…
    Category
    Food
    Distribution
    27 states
  • SevereFDA (Food)·F-1375-2013·2013-05-08

    Buffalo Trace Barbecue Sauce Recalled for Missing Soy and Anchovy Allergens

    Buffalo Trace Distillery is recalling 16 fl. oz. jars of Original Flavor Barbecue Sauce because the label failed to list soy and anchovy allergens.

    Product
    BUFFALO TRACE ORIGINAL FLAVOR BARBEQUE SAUCE Net Wt. 16 fl. oz./532 ml PRODUCED BY: APPLECREEK ORCHARDS LLC P.O. Box 8383 Lexington, KY 40533 BUFFALO TRACE DISTILLERY 113 Great Buffalo Trace Franklin County Frankfort, KY 40601 800-654-8471 e-mail: [email protected]…
    Category
    Food
    Distribution
    27 states
  • SevereNHTSA·13V182000·2013-05-08

    Spartan Motorhome Chassis Recall for Steering Bracket Cracking

    Spartan Motors is recalling 2006-2011 K2, K3, and MM motorhome chassis because steering brackets may crack and detach, causing loss of steering.

    Product
    SPARTAN — SPARTAN K3, MM, K2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1191-2013·2013-05-08

    Medtronic Recalls DBS Therapy Kits Due to Potential Lead Damage

    Medtronic is recalling DBS Therapy for Dystonia Kits because the provided lead cap may damage the lead connector, potentially compromising the device.

    Product
    Medtronic DBS Therapy for Dystonia Kit, models 3317, 3319, 3337 and 3339. Sterile and Non-Pyrogenic. Product Usage: Dystonia Therapy Kit is indicated for unilateral or bilateral stimulation of the internal globus pallidus (GPi) or the subthalamic nucleus (STN) to aid in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1169-2013·2013-05-08

    Hospira GemStar Infusion Pumps Recalled for Unintended Shutdowns

    Hospira Inc. is recalling GemStar infusion pumps because they may shut off during use without warning. The recall affects pumps distributed worldwide.

    Product
    The GemStar Pump is a small and lightweight, single channel infusion device designed for use in the home, in the hospital, or anywhere electronic infusion is required. The GemStar Pump can be powered by AC mains adaptor, rechargeable battery pack, docking station, or two…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-308-2013·2013-05-08

    Hospira Recalls Morphine Sulfate Injection Due to Sterility Concerns

    Hospira Inc. is recalling 26,100 vials of Morphine Sulfate Injection because a loose crimp on the vial cap may compromise sterility.

    Product
    MORPHINE SULFATE — MORPHINE SULFATE (MORPHINE SULFATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V185000·2013-05-08

    Temsa Recalls TS35C Coach Buses Due to Fuel Tank Leak Risk

    Temsa is recalling 172 model year 2011-2013 TS35C coach buses because a production error may cause the fuel tank to leak, posing a fire risk.

    Product
    TEMSA — TEMSA TS35C
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1159-2013·2013-05-08

    Hospira Recalls GemStar Infusion Pumps Due to Battery Data Loss

    Hospira Inc. is recalling GemStar infusion pumps because low battery levels can corrupt history logs and cause an error that prevents the device from being used.

    Product
    GemStar Pump - Battery Product Usage: The GemStar Pump is a small and lightweight, single channel infusion device designed for use in the home, in the hospital, or anywhere electronic infusion is required. The GemStar Pump can be powered by AC mains adaptor, rechargeable…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1368-2013·2013-05-08

    Rich Products Recalls Farm Rich Pizza Dough Stuffed with Mozzarella

    Rich Products Corp is recalling Farm Rich Stuffed Crust Pizza Dippers potentially contaminated with E. coli O121. The recall covers nationwide distribution.

    Product
    Farm Rich Stuffed Crust Pizza Dippers-Pizza Dough Stuffed with Mozzarella Cheese, Net Wt. 27-LBS (10 X 2.7-LB), UPC Code 10041322652659, Product Code 65265; Net Wt. 25-LB (1 X 25-LB) UPC Code 10041322652680, Product Code 65268.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1177-2013·2013-05-08

    Maquet SERVO-i Ventilator Battery Modules Recalled for Shorter Run Time

    Maquet is recalling SERVO-i ventilator battery modules because some units have shorter battery run times than expected.

    Product
    Maquet Getinge Group battery modules for use with Maquet SERVO-i ventilator systems (Part #6487180). Battery for use with the SERVO-i Ventilator System. The SERVO-i Ventilator System is intended for treating and monitoring patients ranging from neonates to adults with…
    Category
    Medical Device
    Distribution
    Distributed nationwide