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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32026–32050 of 39756

  • SevereNHTSA·14V020000·2014-01-28

    Spartan MM Motorhome Chassis Recalled for Sway Bar End Link Defect

    Spartan Motors is recalling 2010-2014 MM motorhome chassis due to a front suspension design that may cause sway bar end links to break, increasing crash risk.

    Product
    SPARTAN — SPARTAN MM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V018000·2014-01-27

    Starcraft Transit Buses Recalled for Alternator Harness Pinch Risk

    Starcraft is recalling 2010-2013 transit buses because a pinched alternator harness could cause vehicle stalling or a fire.

    Product
    STARCRAFT — STARCRAFT STARQUEST, XPRESS, ULTRASTAR, STARLITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V021000·2014-01-27

    Trails West RPM Trailers Recalled for Furnace Fire Risk

    Trails West is recalling 2010-2014 RPM trailers due to a furnace defect that may cause melting and fire.

    Product
    TRAILS WEST — TRAILS WEST RPM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V019000·2014-01-27

    Turtle Top Recalls Ford-Based Transit Buses Due to Electrical Fire Risk

    Turtle Top is recalling 453 Ford-based transit buses because a pinched alternator harness could cause a short circuit, fire, or vehicle stall.

    Product
    TURTLE TOP — TURTLE TOP FORD VAN TERRA, FORD LIMO COACH, FORD ODYSSEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V014000·2014-01-24

    PACCAR Recalls 2012-2014 Kenworth and Peterbilt Trucks for Fire Risk

    PACCAR is recalling 2012-2014 Kenworth K300 and Peterbilt 210/220 trucks because a battery component may conduct electricity when hot, increasing fire risk.

    Product
    PETERBILT — PETERBILT, KENWORTH 210, K300, MODEL 220
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14T001000·2014-01-23

    Lionshead Recalls 39,569 Vail Sport ST LH 99 Trailer Tires

    Lionshead Specialty Tire & Wheel LLC is recalling 39,569 Vail Sport ST LH 99 trailer tires because they may fail or unseat from rims, increasing crash risk.

    Product
    TIRES recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·14086·2014-01-23

    Matrix Fitness Ascent Trainers and Ellipticals Recalled Due to Fire Hazard

    Johnson Health Tech is recalling about 2,800 Matrix Fitness Ascent Trainers and Ellipticals sold to commercial facilities due to a fire hazard from moisture buildup in the power socket.

    Product
    Ascent Trainer® by Matrix and Matrix Fitness Elliptical
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V011000·2014-01-23

    Corn Pro Deckover Flatbed Trailer Recall for Tail Pivot Box Failure

    Cornelius Manufacturing is recalling 2012-2014 Corn Pro Deckover Flatbed Trailers because welded boxes allowing the tail to pivot may fail, increasing accident risk.

    Product
    CORN PRO — CORN PRO DECKOVER FLATBED TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·14089·2014-01-23

    Flushmate III Pressure-Assist Flushing System Recalled for Bursting Hazard

    Flushmate is recalling about 351,000 Flushmate III Pressure-Assist Flushing Systems sold in the U.S. because the units can burst, posing impact and laceration hazards.

    Product
    Flushmate® III Pressure-Assist Flushing System
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1375-2014·2014-01-22

    USPlabs Recalls OxyELITE Pro Powder Due to Serious Liver Damage Reports

    USPlabs is recalling OxyELITE Pro Super Thermo Powder containing Aegeline due to reports of serious liver damage and acute liver failure.

    Product
    USPlabs OxyELITE Pro Super Thermo POWDER Plus Advanced Carnitine Transport System DIETARY SUPPLEMENT Net Wt. 4.6 oz (130 g) GREEN APPLE Manufactured for USPlabs, LLC (Dallas, TX 75220)
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1371-2014·2014-01-22

    USPlabs Recalls OxyELITE Pro Due to Serious Liver Damage Reports

    USPlabs is recalling OxyELITE Pro dietary supplements containing Aegeline due to reports of serious liver damage and acute liver failure.

    Product
    USPlabs OxyELITE Pro Ultra-Intense Thermo Advanced Formula DIETARY SUPPLEMENT Manufactured for USPlabs, LLC (Dallas, TX 75220), sold in the following sizes: 3 count; 90 count; and 180 count.
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1427-2014·2014-01-22

    Del Campo Dried Potato Recall Due to Undeclared Sulfites

    Megabusiness LLC is recalling Del Campo Papa Seca dried potatoes because the product contains undeclared sulfites. The recall covers 39.5 cases distributed in New York, New Jersey, Connecticut, and Illinois.

    Product
    DEL CAMPO PAPA SECA DRIED POTATO NET WT 14 OZ IMPORTED BY MEGABUSINESS PRODUCT OF PERU. UPC CODE 891726000218
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·F-1374-2014·2014-01-22

    USPlabs Recalls OxyELITE Pro Powder Due to Serious Liver Damage Reports

    USPlabs, LLC is recalling OxyELITE Pro Super Thermo Powder containing Aegeline due to reports of serious liver damage and acute liver failure.

    Product
    USPlabs OxyELITE Pro Super Thermo POWDER Plus Advanced Carnitine Transport System DIETARY SUPPLEMENT Net Wt. 4.6 oz (130 g) GRAPE BUBBLEGUM Manufactured for USPlabs, LLC (Dallas, TX 75220)
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1372-2014·2014-01-22

    USPlabs Recalls OxyELITE Pro Powder Due to Serious Liver Damage Risk

    USPlabs is recalling OxyELITE Pro Super Thermo Powder Plus Advanced Carnitine Transport System because it contains Aegeline, which is associated with serious liver damage or acute liver failure.

    Product
    USPlabs OxyELITE Pro Super Thermo POWDER Plus Advanced Carnitine Transport System DIETARY SUPPLEMENT Fruit Punch Manufactured for USPlabs, LLC (Dallas, TX 75220), distributed in the following sizes: Fruit Punch 0.15 oz; Fruit Punch 4.6 oz; and Fruit Punch 5 oz
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1373-2014·2014-01-22

    USPlabs Recalls OxyELITE Pro Powder Linked to Liver Damage

    USPlabs is recalling OxyELITE Pro Super Thermo Powder containing Aegeline due to reports of serious liver damage and acute liver failure.

    Product
    USPlabs OxyELITE Pro Super Thermo POWDER Plus Advanced Carnitine Transport System DIETARY SUPPLEMENT Net Wt. 4.6 oz (130 g) BLUE RASPBERRY Manufactured for USPlabs, LLC (Dallas, TX 75220)
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1370-2014·2014-01-22

    USPlabs Recalls OxyELITE Pro Super Thermo Due to Liver Damage Risk

    USPlabs is recalling OxyELITE Pro Super Thermo dietary supplements containing Aegeline due to reports of serious liver damage and acute liver failure.

    Product
    USPlabs OxyELITE Pro Super Thermo DIETARY SUPPLEMENT Manufactured for USPlabs, LLC (Dallas, TX 75220), distributed in the following sizes: 2 count capsules; 10 count capsules; 21 count capsules; 90 count capsules; and 180 count capsules.
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Drugs)·D-461-2014·2014-01-22

    Hospira Recalls Aminosyn II Amino Acid Injection Due to Particulate Matter

    Hospira is recalling 17,256 containers of Aminosyn II 10% Amino Acid Injection because a human hair was found in the injection port.

    Product
    Aminosyn II, 10%, Sulfite-Free Amino Acid Injection, 500 mL container, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-4164-03, UPC (01) 0 030409 416403 8.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1376-2014·2014-01-22

    USPlabs Recalls OxyELITE Pro Powder Due to Serious Liver Damage Reports

    USPlabs is recalling OxyELITE Pro Super Thermo Powder containing Aegeline due to reports of serious liver damage and acute liver failure.

    Product
    USPlabs OxyELITE Pro Super Thermo POWDER Plus Advanced Carnitine Transport System DIETARY SUPPLEMENT Net Wt. 4.6 oz (130 g) RASPBERRY LEMONADE Manufactured for USPlabs, LLC (Dallas, TX 75220)
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Drugs)·D-649-2014·2014-01-22

    FDA Recalls Misoprostol Tablets Due to Potential Labeling Mixup

    Aidapak Services, LLC is recalling Misoprostol 200 mcg tablets because they may be mislabeled as Propranolol HCl or Sodium Chloride.

    Product
    MISOPROSTOL, Tablet, 200 mcg, Rx only, Distributed by: AidaPak Service, LLC, NDC 59762500801
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-626-2014·2014-01-22

    Aidapak Recalls Tramadol Tablets Due to Potential Labeling Mixup

    Aidapak Services, LLC is recalling 25 mg Tramadol HCl tablets that may be mislabeled as Levothyroxine Sodium 137 mcg.

    Product
    traMADol HCl Tablet, 25 mg (1/2 of 50 mg), Rx only, Distributed by: AidaPak Service, LLC, NDC 57664037708
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-701-2014·2014-01-22

    Aidapak Recalls Cholecalciferol Tablets Due to Potential Labeling Errors

    Aidapak Services, LLC is recalling Cholecalciferol/Calcium/Phosphorus tablets because they may be mislabeled as Promethazine HCl or Valsartan.

    Product
    CHOLECALCIFEROL/ CALCIUM/ PHOSPHORUS Tablet, 120 units/105 mg/81 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 64980015001
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-428-2014·2014-01-22

    Lidocaine/Sodium Chloride Injectable Recalled Due to Sterility Concerns

    Specialty Medicine Compounding Pharmacy is recalling Lidocaine/Sodium Chloride injectable products because sterility cannot be assured after a related product was found non-sterile.

    Product
    LIDOCAINE/SODIUM CHL* 0.4 %/18 % INJECTABLE; all sizes, Rx only, Specialty Medicine Compounding Pharmacy, 350 S Lafayette, South Lyon, MI 48178
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-646-2014·2014-01-22

    Mirtazapine Tablets Recalled for Potential Mislabeling as Isoniazid

    Aidapak Services is recalling Mirtazapine 7.5 mg tablets that may be mislabeled as Isoniazid 300 mg. The error poses a risk of incorrect medication administration.

    Product
    MIRTAZAPINE Tablet, 7.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 59762141509
    Category
    Drug
    Distribution
    4 states