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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19826–19850 of 39655

  • SevereNHTSA·17V527000·2017-08-28

    KME Recalls 2016 Predator Vehicles Due to Steering Defect

    KME is recalling 2016 Predator Pumper, Rescue, and Airport Refueler vehicles because a loose tie rod could cause a complete loss of steering.

    Product
    KME — KME PREDATOR PUMPER, PREDATOR RESCUE, AIRPORT REFUELER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17E048000·2017-08-28

    Ford Recalls Wheel Hub Bearings for 2011-2017 Explorer 4X2 Vehicles

    Ford is recalling certain wheel hub bearing assemblies for 2011-2017 Ford Explorer 4X2 vehicles because they lack a self-retention feature, which could cause the wheel to separate.

    Product
    FORD — FORD EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V531000·2017-08-28

    Triton Recalls 2017 W-25 Trailers Due to Axle Bolt Tightening Defect

    Triton Trailers is recalling 2017 W-25 Single Torsion Axle Trailers because improperly tightened axle mounting bolts may cause the axle to detach, increasing crash risk.

    Product
    TRITON — TRITON W-25
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V529000·2017-08-28

    Ford Recalls 2017 F-150 and Mustang for Air Bag Inflator Defect

    Ford is recalling 2017 F-150 and Mustang vehicles because the passenger air bag inflator may rupture in a crash, potentially causing serious injury or death.

    Product
    FORD — FORD F-150, MUSTANG
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V528000·2017-08-28

    Ford Recalls 2017 Focus Vehicles for Rear Seat Back Weld Defect

    Ford is recalling 2017 Focus vehicles because an insufficient weld on the rear left seat back may reduce its strength, increasing injury risk in a crash.

    Product
    FORD — FORD FOCUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V530000·2017-08-28

    Ford Recalls 2017 Models for Steering Gear Heat Shield Fastener Defect

    Ford is recalling 2017 Explorer, Taurus, and Police Interceptor vehicles because steering gear heat shield fasteners may corrode and detach, potentially causing overheating and increased steering effort.

    Product
    FORD — FORD EXPLORER, TAURUS, POLICE INTERCEPTOR SEDAN, POLICE INTERCEPTOR UTILIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V532000·2017-08-28

    Hyundai Recalls 2017 Ioniq Electric Vehicles for Electronic Power Control Unit Defect

    Hyundai is recalling 2017 Ioniq Electric vehicles because a manufacturing defect in the Electronic Power Control Unit may allow coolant to contact the circuit board, potentially causing a stall and increasing crash risk.

    Product
    HYUNDAI — HYUNDAI IONIQ ELECTRIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·098-2017·2017-08-26

    Blossom Foods Recalls Frozen Meat Products Due to Undeclared Allergens

    Blossom Foods is recalling approximately 15,092 pounds of frozen beef, chicken, and pork products because they contain undeclared soy and wheat allergens.

    Product
    Blossom Foods, LLC — Blossom Foods, LLC Recalls Frozen Meat Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    2 states
  • SevereUSDA FSIS·097-2017·2017-08-26

    Ronald A. Chisholm Recalls Pork Belly Products Lacking Import Inspection

    Ronald A. Chisholm, Ltd. is recalling skinless pork belly products that entered the U.S. without import inspection. The products were distributed to restaurants in Hawaii.

    Product
    Ronald A. Chisholm, Ltd. Recalls Pork Belly Products Produced Without Benefit of Import Inspection
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·17V521000·2017-08-24

    Western Star 4900 Trucks Recalled for Front Axle Spring Defect

    Daimler Trucks North America is recalling 2017-2018 Western Star 4900 trucks because front axle weight capacity may exceed spring capacity, risking axle separation.

    Product
    WESTERN STAR — WESTERN STAR 4900
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1092-2017·2017-08-23

    GEC LX Laxoplex Recalled for Undeclared Anabolic Steroids

    Genetic Edge Compounds LLC is recalling GEC LX Laxoplex dietary supplements because FDA analysis found the product tainted with undeclared anabolic steroids and steroid-like substances.

    Product
    GEC LX Laxoplex 60 capsules Dietary Supplement, 60 count bottle, Manufactured by GEC, McKinney, TX, 75070, UPC: 700580499842
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-3378-2017·2017-08-23

    Laura's Boston Brownies Recalls Bhufit Bars for Listeria Risk

    Laura's Boston Brownies is recalling Bhufit Bar Paleo Double Dark Chocolate Chip bars due to potential Listeria monocytogenes contamination.

    Product
    Bhufit Bar Paleo Double Dark Chocolate Chip; Paleo Egg White Protein: Net Wt 1.6 oz. (45 G)
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-3375-2017·2017-08-23

    Laura's Boston Brownies Recalls Bhufit Bars for Listeria Risk

    Laura's Boston Brownies is recalling Bhufit Bar Apple Chunk Cinnamon Nutmeg bars due to potential Listeria monocytogenes contamination.

    Product
    Bhufit Bar Apple Chunk Cinnamon Nutmeg; Vegan Organic Pea Protein Net Wt. 1.6 oz (45G)
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-3383-2017·2017-08-23

    Laura's Boston Brownies Recalls Bhufit Bars for Listeria Risk

    Laura's Boston Brownies is recalling Bhufit Bar Dark Chocolate Coconut Almond products due to potential Listeria monocytogenes contamination.

    Product
    Bhufit Bar Dark Chocolate Coconut Almond
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Drugs)·D-1087-2017·2017-08-23

    Biotech Underground Tri-Ton Hardcore Formula Recalled for Unapproved Ingredients

    Dynamic Technical Formulations is recalling Biotech Underground Tri-Ton Hardcore Formula capsules because FDA testing found unapproved drug ingredients.

    Product
    Biotech Underground Tri-Ton Hardcore Formula capsules, 90-count bottle, Distributed by: Dynamic Technical Formulations 12850 Hwy 9 Suite 600-441 Alpharetta, GA 30004
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-3376-2017·2017-08-23

    Laura's Boston Brownies Recalls Bhufit Protein Bars for Listeria Risk

    Laura's Boston Brownies is recalling specific Bhufit protein bars due to potential Listeria monocytogenes contamination. Consumers should check lot codes and stop eating the product.

    Product
    Bhufit Bar Chocolate Tart Cherry Pistachio; Vegan Organic Pea Protein Net Wt. 1.6 oz. (45G)
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-3379-2017·2017-08-23

    Laura's Boston Brownies Recalls Peanut Butter Protein Bars for Listeria Risk

    Laura's Boston Brownies is recalling Bhufit Bar Peanut Butter White Chocolate Vegan Organic Pea Protein bars due to potential Listeria monocytogenes contamination.

    Product
    Bhufit Bar Peanut Butter White Chocolate; Vegan Organic Pea Protein: Net Wt. 1.6 oz. (45G)
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-3381-2017·2017-08-23

    Laura's Boston Brownies Recalls Bhufit Bars for Listeria Risk

    Laura's Boston Brownies is recalling Bhufit Vanilla Almond Cashew bars due to potential Listeria monocytogenes contamination. Consumers should stop eating these products.

    Product
    Bhufit Bar Vanilla Almond Cashew, Primal Grass-Fed Whey Protein: Net. Wt. 1.6 oz. (45G)
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-3377-2017·2017-08-23

    Laura's Boston Brownies Recalls Peanut Butter Chocolate Chip Bars for Listeria Risk

    Laura's Boston Brownies is recalling Bhufit Bar Peanut Butter Chocolate Chip bars due to potential Listeria monocytogenes contamination. The recall affects 62,951 bars distributed in the US.

    Product
    Bhufit Bar Peanut Butter Chocolate Chip; Vegan Organic Pea Protein;Net Wt. 1.6 oz. (45G)
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-3367-2017·2017-08-23

    NatureAll Acidophilus-Plus Recalled for Undeclared Milk Allergens

    NatureAll is recalling Acidophilus-Plus dietary supplements because they contain undeclared milk allergens, including colostrum, dried yogurt, and whey.

    Product
    Acidophilus-Plus, No. 102, 90 Capsules, Dietary Supplement,
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3038-2017·2017-08-23

    Boston Scientific Recalls Emblem MRI S-ICD Devices Due to Energy Delivery Risk

    Boston Scientific is recalling approximately 9,200 Emblem MRI S-ICD devices because memory corruption may cause the device to deliver an atypical amount of energy.

    Product
    EMBLEM MRI S-ICD Model 219, Subcutaneous-Implantable Cardioverter Defibrillator, Rx. Product Usage: The S-ICD system is intended to provide defibrillation therapy for the treatment of life-threatening ventricular tachyarrhythmias in patients who do not have symptomatic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1085-2017·2017-08-23

    Hardcore Formulations Recalls D-ZINE Rapid Size and Strength Capsules

    Hardcore Formulations is recalling D-ZINE Rapid Size and Strength capsules because they contain unapproved active ingredients.

    Product
    D-ZINE Rapid Size and Strength capsules, 10mgs, 90 count bottle, Hardcore Formulations, UPC: 7 48252 86193 1
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3034-2017·2017-08-23

    Cenorin ThermaSure Medical Device Dryers Recalled for Overheating Terminal Block

    Cenorin, LLC is recalling 18 ThermaSure Series 1000 medical device dryers because a manufacturing defect causes the terminal block to overheat, char, or burn.

    Product
    ThermaSure(TM), a CENORIN(TM) product, SERIES 1000 MEDICAL DEVICE DRYER: (a) Model 1009; (b) Model 1010 Forced air dryer for medical devices
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·095-2017·2017-08-23

    USDA Recalls Chicken Skewers Due to Possible Listeria Contamination

    Expresco Foods is recalling approximately 20,446 pounds of imported chicken skewer products that may be contaminated with Listeria monocytogenes.

    Product
    Expresco Foods Inc. Recalls Chicken Skewer Products Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    7 states