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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25126–25150 of 39703

  • SevereFDA (Drugs)·D-0635-2016·2016-02-03

    Sentara Recalls Nafcillin Bags Due to Sterility Assurance Concerns

    Sentara Enterprises is recalling 28 bags of Nafcillin 2GM in NS due to a lack of assurance of sterility. The affected product was distributed in Virginia and North Carolina.

    Product
    Nafcillin 2GM in NS, Packaged in 50ML Homepumps, Rx Only. SENTARA HOME HEALTH SENTARA RX, 535 Independence Pkwy ste.300, Chesapeake, VA 23320-5176.
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0618-2016·2016-02-03

    Sentara Recalls Intralipid Fat Emulsion Due to Sterility Assurance Issues

    Sentara Enterprises is recalling specific lots of Intralipid fat emulsion because the product's sterility cannot be guaranteed. The affected bags were distributed in Virginia and North Carolina.

    Product
    INTRALIPID (fat emulsion), Packaged in a) 27ML Homepumps, b) 125ML Homepumps, c) 1800ML Homepumps, d) 2000ML Homepumps e) 2350ML Homepumps, and f) 2800ML Homepumps, Rx Only. SENTARA HOME HEALTH SENTARA RX, 535 Independence Pkwy ste.300, Chesapeake, VA 23320-5176.
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0621-2016·2016-02-03

    Sentara Recalls Ceftriaxone Infusions Due to Sterility Concerns

    Sentara Enterprises is recalling specific lots of Ceftriaxone in NS Homepumps because product sterility cannot be guaranteed. The recall affects 82 bags distributed in Virginia and North Carolina.

    Product
    CEFTRIAXONE in NS, Packaged as a) 1GM in 50ML Homepumps, b) 2GM in 100ML Homepumps, and c) 8GM in 200ML Homepumps, Rx Only. SENTARA HOME HEALTH SENTARA RX, 535 Independence Pkwy ste.300, Chesapeake, VA 23320-5176.
    Category
    Drug
    Distribution
    2 states
  • SevereNHTSA·16V058000·2016-02-02

    Highland Ridge RV Recalls Travel Trailers With Underrated Safety Chains

    Highland Ridge RV is recalling 2015-2016 travel trailers because the safety chains are rated for less weight than the trailers' gross vehicle weight rating.

    Product
    HIGHLAND RIDGE TT — HIGHLAND RIDGE TT, HIGHLAND RIDGE FW ROAMER, HIGHLANDER, MESA RIDGE, JOURNEYER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16T002000·2016-02-01

    Bridgestone Recalls Trailer Tires Due to Tread Separation Risk

    Bridgestone is recalling specific FS561 trailer tires manufactured in 2015-2016 because tread separation could cause a sudden loss of air pressure and increase crash risk.

    Product
    TIRES recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V052000·2016-02-01

    Snake River Recalls 2015-2016 Horse Trailers Due to Axle Weld Failure

    Snake River Trailer Company is recalling 2015-2016 Horse Trailers because a weld on the rear axle may fail, causing the wheel assembly to separate and increasing crash risk.

    Product
    SNAKE RIVER — SNAKE RIVER HORSE TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·012-2016·2016-01-30

    Noble Spoon Recalls Uninspected Chicken and Beef Entrees

    The Noble Spoon is recalling approximately 289 pounds of beef and chicken entrees produced without federal inspection. The products were sold in Marin and Sonoma counties, California.

    Product
    The Noble Spoon Recalls Chicken and Beef Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·16V047000·2016-01-29

    Chrysler Recalls 2008-2009 Minivans and Journey for Air Bag Defect

    Chrysler is recalling 110,482 vehicles because corroded air bag control units may fail to deploy or deploy unexpectedly, increasing crash risk.

    Product
    DODGE — DODGE, CHRYSLER GRAND CARAVAN, TOWN AND COUNTRY, JOURNEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V051000·2016-01-29

    C&B Quality Trailer Works Recalls Horse Trailers Due to Axle Weld Failure

    C&B Quality Trailer Works is recalling 2015-2016 horse trailers because a weld on the rear axle may fail, causing the wheel assembly to separate and increasing crash risk.

    Product
    C&B QUALITY TRAILER WORKS — C&B QUALITY TRAILER WORKS HORSE TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V045000·2016-01-28

    Volkswagen Recalls 2015 Tiguan and Audi Q5 for Air Bag Defect

    Volkswagen is recalling 2015 Tiguan and Audi Q5 vehicles because seat-mounted air bag inflators may rupture in a crash, potentially causing serious injury or death.

    Product
    AUDI — AUDI, VOLKSWAGEN Q5, TIGUAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V044000·2016-01-28

    Chrysler and Dodge Minivans Recalled for Windshield Mounting Defect

    Chrysler is recalling 2014-2016 Town and Country and Grand Caravan minivans because expired primer may allow the windshield to dislodge in a crash.

    Product
    CHRYSLER — CHRYSLER, DODGE TOWN AND COUNTRY, GRAND CARAVAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·16084·2016-01-28

    Tristar Recalls AquaRug Shower Rugs Due to Fall Hazard

    Tristar Products is recalling AquaRug shower rugs because the suction cups can fail, causing slips and falls. Consumers should stop using the rugs and contact the company for a free replacement.

    Product
    AquaRug shower rugs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V043000·2016-01-28

    Dodge Charger Recall: Tire Jack Failure Risk Without Wheel Chocks

    Chrysler is recalling 2011-2016 Dodge Chargers because the body-side sill may fail if the vehicle is lifted with the supplied tire jack without chocking the wheels, increasing injury risk.

    Product
    DODGE — DODGE CHARGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V046000·2016-01-28

    Ford Recalls 2016 E-350 and E-450 Vans for Trailer Brake Failure

    Ford is recalling 2016 E-350 and E-450 vans with 6.8L engines and trailer brake controllers because the braking system may fail, increasing stopping distance.

    Product
    FORD — FORD E-450, E-350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·16725·2016-01-28

    RNG Recalls 100-Watt Bendable Solar Panels Due to Fire Hazard

    RNG Group Inc. is recalling Renogy 100-watt bendable solar panels because they can overheat and cause fires. Consumers should stop using the panels and return them for free replacements.

    Product
    100-watt bendable solar panels
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0660-2016·2016-01-27

    St. Jude Medical Recalls Optisure Dual Coil Defibrillation Leads

    St. Jude Medical is recalling Optisure Dual Coil Defibrillation Leads due to potential insulation cuts in the SVC shock coil.

    Product
    Optisure Dual Coil Defibrillation Leads, Model No. LDA220, LDA220Q, LDA230Q, LDP220Q. St. Jude Medical. Designed for long term attachment to an Implantable Cardioverter Defibrillator (ICD).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0631-2016·2016-01-27

    Arkray SPOTCHEM II Reagent Test Strips Recalled for Glucose Error

    Arkray Factory USA is recalling specific lots of SPOTCHEM II test strips because they may display inaccurate glucose results for high values.

    Product
    arkray SPOTCHEM II Basic Panel - 1 Reagent test strips, Product # 11726, MEDTEST DX Catalog # 77484. Calcium, Blood Urea Nitrogen, Glucose, Albumin, Creatinine. For the in vitro quantitative determination of calcium, blood urea nitrogen (BUN), glucose, albumin, and…
    Category
    Medical Device
    Distribution
    8 states
  • SevereFDA (Devices)·Z-0665-2016·2016-01-27

    MWT Materials Recalls Accusorb MRI Radio Frequency Shielding Products

    MWT Materials, Inc. is recalling Accusorb MRI radio frequency shielding blankets and body-part covers because they may overheat and lead to patient injury when not used correctly.

    Product
    Accusorb MRI MAC7004 Part Number: MRI-04 MRI-Poncho Product Usage: Radio frequency shielding blankets and body-part covers for the MRI environment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0577-2016·2016-01-27

    Energique Joint Pain Spray Recalled for Microbial Contamination

    Grato Holdings is recalling Energique Joint Pain & Stiffness Relief Topical Spray due to microbial contamination. Testing revealed out-of-specification results for total aerobic microbiological count.

    Product
    Energique, Homeopathic Remedy, Joint Pain & Stiffness Relief, Topical Spray, 1 fl oz (30 ml) bottles, NDC 44911-0133-1, Dist. by Energique, Inc., Woodbine, IA; ALSO LABELED AS --- Liddell Laboratories, Joint Pain & Stiffness Relief, Topical Homeopathic Spray, NDC 50845-0218-1…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·009-2016 expansion·2016-01-27

    Home Maid Ravioli Recalled for Undeclared Allergens and Lack of Inspection

    Home Maid Ravioli Company is recalling approximately 38,950 pounds of meat and poultry ravioli and pasta products due to undeclared allergens and lack of federal inspection.

    Product
    Home Maid Ravioli Company, Inc. Recalls Meat and Poultry Ravioli and Pasta Products Produced Without Benefit of Inspection and Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0581-2016·2016-01-27

    Pine Pharmaceuticals Recalls Bevacizumab Syringes Due to Silicone Oil Particulates

    Pine Pharmaceuticals is recalling Bevacizumab syringes for intravitreal use because they contain silicone oil microdroplets.

    Product
    Bevacizumab 1.25 mg/0.05 mL in 3/10 mL 31 G 5/16" Syringe for intravitreal Rx -- Pine Pharmaceuticals, 100 Colvin Woods Pkwy Suite 300, Tonawanda, NY 14150.
    Category
    Drug
    Distribution
    Distributed nationwide