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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31876–31900 of 39756

  • SevereFDA (Food)·F-1469-2014·2014-02-12

    Triarco Red Lightening Drink Granulation Recalled for Chloramphenicol Contamination

    Triarco Industries is recalling Red Lightening Drink Granulation due to potential contamination with Chloramphenicol. The product is for manufacturing use only.

    Product
    Triarco Industries, LLC an Innophos company Red Lightening Drink Granulation Notice- For manufacturing Use Only Not for Resale
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-1471-2014·2014-02-12

    Triarco Activessence Recalled for Potential Chloramphenicol Contamination

    Triarco Industries is recalling Activessence, a manufacturing ingredient, due to potential contamination with Chloramphenicol.

    Product
    Triarco Industries, LLC an Innophos company Activessence (R) Notice- For Manufacturing Use Only Not for Resale
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Drugs)·D-1061-2014·2014-02-12

    Teva Recalls Valacyclovir Tablets Due to Potential Foreign Tablet Fragments

    Teva Pharmaceuticals USA is recalling Valacyclovir Hydrochloride 1 g tablets because bottles may contain fragments of Pravastatin tablets.

    Product
    Valacyclovir Hydrochloride Tablets, 1 g, 30 count bottle, Rx only manufactured in Israel by Teva Pharmaceuticals Ind., LTD, Jerusalem, Israel, Manufactured for Teva Pharmaceuticals USA, Sellersville, PA. NDC #0093-7259-56
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1470-2014·2014-02-12

    Triarco Recalls Green Lightening Drink Granulation Due to Chloramphenicol Contamination

    Triarco Industries is recalling Green Lightening Drink Granulation that may be contaminated with Chloramphenicol. The product is for manufacturing use only.

    Product
    Triarco Industries, LLC an Innophos company Green Lightening Drink Granulation Notice - For Manufacturing Use Only Not for Resale
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Drugs)·D-1057-2014·2014-02-12

    Baxter Recalls Nitroglycerin Injection Due to Particulate Matter

    Baxter Healthcare is recalling 49,932 vials of Nitroglycerin in Dextrose Injection because particulate matter was found in one vial.

    Product
    NITROGLYCERIN IN DEXTROSE — NITROGLYCERIN IN DEXTROSE (NITROGLYCERIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0905-2014·2014-02-12

    Medtronic Aquamantys3 Pump Generator Recalled for Electrical Safety Defect

    Medtronic is recalling 242 Aquamantys3 Pump Generators because internal protection circuitry may fail, exposing patients to DC voltage during surgery.

    Product
    Medtronic Advanced Energy Aquamantys3 Pump Generator; Product Catalog Number: 10-1357 (Generator assembly), 40-404-1(as shipped, including accessories) The Aquamantys3 System combines radio frequency (RF) energy and saline to reduce blood loss during and after surgical…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V052000·2014-02-12

    Nissan Recalls 2012-2014 Frontier Vehicles for Wiring Fire Risk

    Nissan is recalling 2012-2014 Frontier vehicles because an incorrectly installed circuit breaker may cause a wire harness to contact a metal bolt, potentially leading to an electrical short and fire.

    Product
    NISSAN — NISSAN FRONTIER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1067-2014·2014-02-12

    Health & Beyond Tranquility Supplement Recalled for Unapproved Prescription Drugs

    Health & Beyond is recalling Tranquility dietary supplements because they contain unapproved prescription drugs, Doxepin and Chlorpromazine.

    Product
    HEALTH & BEYOND DR. LARRY'S Tranquility DIETARY SUPPLEMENT 30 Capsules Manufactured for: Health & Beyond 7050 W Palmetto Pk Rd Boca Raton, FL 33433.
    Category
    Drug
    Distribution
    7 states
  • SevereFDA (Drugs)·D-1066-2014·2014-02-12

    Apothecure Recalls Sterile Compounded Products Due to Sterility Assurance Concerns

    Apothecure, Inc. is recalling all lots of sterile compounded products within expiry due to lack of sterility assurance identified during an FDA inspection.

    Product
    The firm is recalling all lots of sterile products compounded by the pharmacy that are within expiry.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0908-2014·2014-02-12

    Medtronic Mosaic Aortic Obturator Recalled for High Transvalvular Gradients

    Medtronic is recalling Mosaic Aortic Obturators used with Mosaic Porcine Aortic Bioprostheses due to higher-than-expected transvalvular gradients after implant.

    Product
    Product Name: Model 7305- Mosaic Aortic Obturator The Mosaic Aortic Obturators are used with the Mosaic Porcine Aortic Bioprostheses.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V070000·2014-02-11

    Monroe Truck Equipment Recalls Sure Power Battery Equalizers and Converters

    Monroe Truck Equipment is recalling specific Chevrolet and Ford vehicles equipped with Sure Power battery equalizers or DC-DC converters due to a fire risk caused by a defective potting compound.

    Product
    CHEVROLET — CHEVROLET, FORD TAHOE, F-350, C7500NA, F-450 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V055000·2014-02-11

    Freedom Motors Recalls Wheelchair-Accessible Vans Due to Rear Axle Cracks

    Freedom Motors is recalling certain 2008-2010 Dodge, Chrysler, and 2009 Volkswagen wheelchair-accessible vans because the rear axle may crack and fail, increasing crash risk.

    Product
    DODGE — DODGE, VOLKSWAGEN, CHRYSLER GRAND CARAVAN, ROUTAN, TOWN AND COUNTRY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V066000·2014-02-10

    Elkhart Transit Bus Recall for Alternator Harness Pinch Hazard

    Elkhart Coach is recalling 2010-2013 ECI and ECII transit buses because a pinched alternator harness could cause vehicle stalling or a fire.

    Product
    ELKHART — ELKHART ECI, ECII
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V046000·2014-02-10

    Mitsubishi Fuso Trucks Recalled for Transmission Debris Contamination

    Mitsubishi Fuso is recalling 2012-2014 trucks because debris in the transmission fluid may cause the vehicle to stall, increasing crash risk.

    Product
    MITSUBISHI FUSO — MITSUBISHI FUSO FEC52, FEC92, FGB72, FEC72
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V048000·2014-02-10

    Elkhart ECII Transit Bus Recall for Electrical Fire Risk

    Elkhart Coach is recalling 2009-2010 ECII transit buses due to a defect in electric door actuators that may cause circuit boards to overheat and start a fire.

    Product
    ELKHART — ELKHART ECII
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V047000·2014-02-10

    GM Recalls Vehicles for Ignition Switch Airbag Deployment Risk

    General Motors is recalling approximately 2.19 million vehicles because a defective ignition switch may turn off the engine, preventing airbags from deploying in a crash.

    Product
    CHEVROLET — CHEVROLET, SATURN, PONTIAC HHR, SKY, SOLSTICE, G5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V049000·2014-02-10

    EZ Loader Recalls 2013-2014 Boat Trailers Due to Wheel Cracking

    EZ Loader is recalling 2013-2014 boat trailers because specific trailer wheels may crack and separate, potentially causing a crash.

    Product
    EZ LOADER — EZ LOADER BOAT TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·012-2014·2014-02-08

    Wyoming Firm Recalls Beef Jerky Due to Processing Deviation

    Wyoming Authentic Products LLC is recalling 365 pounds of beef jerky sold in four states and online due to a processing deviation.

    Product
    Wyoming Authentic Products LLC — Wyoming Firm Recalls Beef Jerky Products Due to a Processing Deviation
    Category
    Food
    Distribution
    4 states
  • SevereNHTSA·14V040000·2014-02-06

    Ford F-550 Transit Bus CNG Tank Bracket Recall

    Almared is recalling 2011-2012 Ford F-550 buses converted to CNG because fuel tank brackets may break, risking a crash or fire.

    Product
    FORD — FORD F-550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V041000·2014-02-06

    Marathon Recalls Prevost Motorcoaches Due to Battery Fire Risk

    Marathon Coach is recalling 450 Prevost H3 and XL motorcoaches because battery components may conduct electricity and cause fires.

    Product
    PREVOST — PREVOST H3, XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1049-2014·2014-02-05

    Alexion Recalls Soliris Vials Due to Visible Particulate Matter

    Alexion Pharmaceuticals is recalling 21,661 vials of Soliris (eculizumab) because they failed an appearance test for visible particles.

    Product
    SOLIRIS — SOLIRIS (ECULIZUMAB)
    Category
    Drug
    Distribution
    Distributed nationwide