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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37126–37150 of 39777

  • SevereNHTSA·12V396000·2012-08-10

    B & M Recalls 2012 HAUL-RITE Boat Trailers Due to Wheel Torque Defect

    B & M Manufacturing is recalling 2012 HAUL-RITE boat trailers because improperly specified wheels may not tighten correctly, risking wheel separation.

    Product
    HAUL-RITE — HAUL-RITE ABT78-TDM, ABT66-TDM, TRN63-HD, ABT78-HD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V392000·2012-08-10

    Ducati Recalls 2012-2013 1199 Panigale Motorcycles for Fire Risk

    Ducati is recalling 2012-2013 1199 Panigale motorcycles because the exhaust butterfly valve bowden cable cover could melt or burn, leading to smoke or fire.

    Product
    DUCATI — DUCATI 1199 PANIGALE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12E029000·2012-08-10

    Valeo Recalls Engine Cooling Fans for Certain BMW Models

    Valeo is recalling aftermarket engine cooling fans for specific BMW models because a component may overheat and cause a fire.

    Product
    BMW — BMW 3 SERIES, 5 SERIES, 6 SERIES, 7 SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·12244·2012-08-09

    GE Recalls Dishwashers Due to Electrical Fire Hazard

    GE is recalling approximately 1.3 million dishwashers sold between 2006 and 2009 because an electrical failure in the heating element can cause fires.

    Product
    GE, GE Adora™, GE Eterna™, GE Profile™ and Hotpoint®, Dishwashers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1440-2012·2012-08-08

    VistaPharm Recalls Xactdose Phenytoin Oral Suspension Due to Container Defects

    VistaPharm is recalling Xactdose Phenytoin Oral Suspension because defective container lids allow moisture loss, potentially causing viscosity and assay failures.

    Product
    Xactdose Phenytoin Oral Suspension, USP 125 mg/5mL, supplied in 5 mL unit dose cups, VISTAPHARM, Largo, FL NDC 66689-036-50
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2113-2012·2012-08-08

    Sunrise Medical Recalls Padded Swing Away Arm Rests Due to Injury Reports

    Sunrise Medical is recalling 14,035 Padded Swing Away Arm Rests for specific wheelchair models because reports indicate injury when the armrest is used to support full body weight.

    Product
    Padded Swing Away Arm Rest with Receiver; Uses on wheelchair models: Quickie Q7 (EIR4), GT (EIR3), GTi (EIT4) and Zippie Zone (EIRZ1). Product Usage: To empower physically challenged persons by providing a means of mobility. This includes temporary and permanent…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1429-2012·2012-08-08

    Eagle Pharmaceuticals Recalls Argatroban Injection Due to Visible Particulates

    Eagle Pharmaceuticals is recalling specific lots of Argatroban Injection after a hospital reported crystalline particulates and fibers in a vial.

    Product
    Argatroban Injection 50 mg per 50ml (1 mg per ml) For Intravenous Infusion Only, a) Single Use Vial (NDC 42367-203-07), b) 10 Single Use Vials(NDC 42367-203-84), Rx Only, Manufactured by: Cipla LTD, India, Manufactured for: Eagle Pharmaceuticals, Inc. Woodcliff Lake, NJ…
    Category
    Drug
    Distribution
    1 state
  • SevereNHTSA·12V390000·2012-08-08

    Altec Aerial Device Vehicles Recalled for Steering Defect

    Altec is recalling 2012 aerial device vehicles because a torsion bar issue may cause steering deviation over bumps, increasing crash risk.

    Product
    ALTEC — ALTEC AT235P, AT37-G, AT235, AT200A
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2107-2012·2012-08-08

    Smiths Medical Medfusion 4000 Syringe Infusion Pump Software Recall

    Smiths Medical is recalling Medfusion 4000 Syringe Infusion Pumps due to a software anomaly that causes device history log corruption and triggers a Watchdog Fail-Safe alarm.

    Product
    Smiths Medical, Medfusion¿ Syringe Infusion Pump, Model 4000, Software Version V1.0 & V1.1, Reorder Numbers 4000-0100-50, 4000-0100-95, 4000-0101-50, 4000-0101-51, and 4000-0101-78. Designed for use in care areas for the administration of fluids requiring precisely…
    Category
    Medical Device
    Distribution
    1 state
  • SevereNHTSA·12V389000·2012-08-08

    Winnebago and Itasca Motor Homes Recalled for Propane Tubing Defect

    Winnebago is recalling 2012-2013 motor homes because scored copper propane tubing may fail, risking fire or explosion.

    Product
    WINNEBAGO — WINNEBAGO, ITASCA COMMERCIAL VEHICLE, REYO, VIEW PROFILE, VISTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1435-2012·2012-08-08

    Dr. Reddy's Ciprofloxacin Tablets Recalled for Foreign Tablet Contamination

    Dr. Reddy's is recalling Ciprofloxacin Tablets due to complaints of mislabeled bottles containing foreign tablets.

    Product
    Dr. Reddy's Ciprofloxacin Tablets, USP 500 mg*, 500 Tablets, Rx only, Mfd. By: Dr. Reddy's Laboratories Limited, Bachepalli - 502 325 INDIA, NDC 55111-127-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1820-2012·2012-08-08

    Spillson's Big Sicilian Sandwich Recalled for Undeclared Yellow #5

    Spillson's, Ltd. is recalling 17 units of The Big Sicilian Sandwich due to undeclared Yellow #5 in the pepper ingredient, posing a risk to sensitive individuals.

    Product
    Spillson's Ltd. The Big Sicilian Sandwich Nt. Wt. 7oz
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-2092-2012·2012-08-08

    Zimmer Recalls Nextgen Knee Replacement Jaw Instruments Due to Fracture Risk

    Zimmer Inc. is recalling Nextgen Complete Knee Solution replacement jaws because the spring clip may fracture or fall off during use, potentially leaving fragments in the surgical site.

    Product
    Nextgen Complete Knee Solution Replacement Jaw for Use with Femoral and Provisional Impactor/Extractor, REF 00-5901-026-40, Non-Sterile Zimmer, Warsaw Indiana The instrument is attached to the femoral implant or provisional to aid in positioning and inserting the components.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V388000·2012-08-08

    GM Recalls 2003-2004 Chevrolet Express and GMC Savana for Fuel Leak Risk

    General Motors is recalling 2003-2004 Chevrolet Express and GMC Savana vans in specific states due to a fuel filler pipe corrosion issue that could cause a fire.

    Product
    CHEVROLET — CHEVROLET, GMC EXPRESS, SAVANA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12T021000·2012-08-08

    Hercules Recalls H502 Truck Tires Due to Sidewall Separation Risk

    Hercules Tire & Rubber Company is recalling specific H502 truck tires due to a manufacturing defect that may cause sidewall separation and increase crash risk.

    Product
    TIRES:SIDEWALL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1809-2012·2012-08-08

    Andante Dairy Cheese Recalled for Lack of Proper Pasteurization

    Andante Dairy is recalling multiple lots of cheese due to a lack of proper pasteurization, which could allow dangerous pathogens to survive.

    Product
    Multiple lots of cheese produced by Andante Dairy, Petaluma, CA; Sold in 5 oz to 8 oz sizes with no code date or variety information on packaged. Varieties include: Largo, a triple-creme cow's milk, and Picolo, a triple-creme cow's milk. Also made with cow's milk…
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Drugs)·D-1433-2012·2012-08-08

    Bayer Recalls Estradiol Hemihydrate Powder Due to Cross Contamination

    Bayer HealthCare Pharmaceuticals is recalling Estradiol Hemihydrate M20 EP/USP Powder due to cross contamination with another product. The affected lot was distributed in Kansas and California.

    Product
    Estradiol Hemihydrate M20 EP/USP Powder, packaged in a) 1.5 kg and b) 2.5 kg fiber drums, Rx only, Art. No. 165811, Bayer Pharma AG, D-13342 Berlin.
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Drugs)·D-1434-2012·2012-08-08

    Dr. Reddy's Recalls Amlodipine and Benazepril Capsules Due to Foreign Tablets

    Dr. Reddy's is recalling Amlodipine Besylate and Benazepril Hydrochloride capsules because bottles were mislabeled and contained foreign Ciprofloxacin tablets.

    Product
    AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE — AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE (AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide