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.

Filters

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All agenciesFDA (Food)FDA (Drugs)FDA (Devices)USDA FSISCPSCNHTSAEPA

Category

All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

Clear filters

17976–18000 of 39605

  • SevereFDA (Devices)·Z-1903-2018·2018-06-06

    Heartware Medtronic HVAD System Recalled for Transient Electrical Interruptions

    Heartware is recalling HVAD System components due to possible transient electrical connection interruptions that may cause unexpected beeping or power switching.

    Product
    Heartware Medtronic HVAD System for cardiac use. Including the following parts: (a) Controller / Controller Kits, Product numbers: 1400, 1401, 1403, 1407, 1420 (b) DC Adapter, Product numbers: 1435, 1440 (c) AC Adapter, Product numbers: 1425, 1430 (d) Battery Pack…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2038-2018·2018-06-06

    Torax Medical Recalls LINX Reflux Management System Implant Clasps

    Torax Medical is recalling LINX Reflux Management System implant clasps because a manufacturing defect may allow a bead to separate from the wire link, potentially rendering the device discontinuous or open.

    Product
    LINX Reflux Management System, Implant Clasp, 12-17 Bead, 0.7T, Product Code LXC-xx, sterile, Rx only. Labeled as: a. Product Code LXC-12; b. Product Code LXC-13; c. Product Code LXC-14; d. Product Code LXC-15; e. Product Code LXC-16; f. Product Code LXC-17…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·045-2018·2018-06-04

    Goodman Recalls Fully Cooked Ground Beef Due to Plastic Contamination

    Goodman Food Products is recalling approximately 34,400 pounds of fully cooked ground beef products due to possible contamination with hard, white plastic.

    Product
    Goodman Food Products, Texas Inc. — Goodman Food Products Recalls Fully Cooked Ground Beef Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    2 states
  • SevereNHTSA·18V361000·2018-06-01

    Forest River Recalls 2019 Wildcat Trailers Due to Underrated Tires

    Forest River is recalling 2019 Wildcat recreational trailers because they were equipped with underrated tires, which could lead to tire failure and increase the risk of a crash.

    Product
    FOREST RIVER — FOREST RIVER WILDCAT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V357000·2018-06-01

    2019 Forest River and Coachmen Motorhomes Recalled for Rear Axle Defect

    Forest River is recalling 2019 Forester, Sunseeker, and Coachmen Leprechaun and Freelander motorhomes because rear axle U-Bolts may loosen, increasing crash risk.

    Product
    COACHMEN — COACHMEN, FOREST RIVER LEPRECHAUN, SUNSEEKER, FORESTER, FREELANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V366000·2018-06-01

    Forest River Recalls Transit Buses Due to Rear Axle U-Bolt Defect

    Forest River is recalling certain 2018-2019 transit buses because insufficiently tightened rear axle U-bolts may break, causing the axle to separate and increasing crash risk.

    Product
    STARCRAFT BUS — STARCRAFT BUS, FOREST RIVER, ELKHART SENATOR II MVP, ALLSTAR MVP, SENATOR II, ROCKPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V369000·2018-06-01

    Volkswagen and Audi Recall 2018 Models for Brake Caliper Coating Defect

    Volkswagen and Audi are recalling 2018 models because brake caliper pistons may have insufficient coating, potentially reducing braking performance and increasing crash risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN, AUDI PASSAT, GTI, GOLF, SQ5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V364000·2018-06-01

    Jayco Recalls 2018-2019 Fifth-Wheel Trailers Due to Propane Strap Defect

    Jayco is recalling 2018-2019 fifth-wheel trailers because the propane tank strap may separate, increasing the risk of a crash or fire.

    Product
    JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL, JAYCO TRAVEL TRAILER, JAYCO SEISMIC, NORTH POINT, PINNACLE, EAGLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V363000·2018-06-01

    Kia Recalls 507,587 Vehicles Due to Air Bag Control Unit Short Circuit Risk

    Kia is recalling 507,587 vehicles because the air bag control unit may short circuit, preventing frontal air bags and seat belt pretensioners from deploying in a crash.

    Product
    KIA — KIA FORTE, SEDONA, OPTIMA, OPTIMA HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V362000·2018-06-01

    Starcraft Telluride Fifth-Wheel Trailer Propane Strap Recall

    Starcraft is recalling 2019 Telluride fifth-wheel trailers because the propane tank strap may separate, increasing the risk of a crash or fire.

    Product
    STARCRAFT RV FW — STARCRAFT RV FW TELLURIDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V367000·2018-06-01

    MORryde Recalls 2018 Ford E-450 Chassis Due to Loose U-Bolts

    MORryde is recalling 2018 Ford E-450 chassis modified for transit bus use because insufficiently tightened U-bolts may allow the rear axle to separate, increasing crash risk.

    Product
    FORD — FORD E-450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E037000·2018-05-31

    Dorman Front Control Arms Recalled for Potential Steering Loss

    Dorman is recalling specific front control arms where a ball stud may pull through the steering knuckle, causing partial loss of steering.

    Product
    SUSPENSION:FRONT:CONTROL ARM recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V358000·2018-05-31

    GM Recalls 2015-2018 Vehicles for Fuel Pump Fire Risk

    General Motors is recalling specific 2015-2018 GMC, Chevrolet, Buick, and Cadillac vehicles because a fuel pump may detach and cause a leak, increasing fire risk.

    Product
    GMC — GMC, CHEVROLET, BUICK CANYON, MALIBU, ENVISION, ACADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V359000·2018-05-31

    Kenworth Recalls 2019 T270 and T370 Trucks for Axle Nut Issue

    PACCAR is recalling 2019 Kenworth T270 and T370 vehicles because over-tightened rear axle nuts may cause bearing failure or fire, increasing crash risk.

    Product
    KENWORTH — KENWORTH T270, T370
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0821-2018·2018-05-30

    FDA Recalls Rhino 69 Extreme 50000 for Undeclared Tadalafil

    The FDA is recalling Rhino 69 Extreme 50000 capsules because they contain undeclared tadalafil, an unapproved drug with unestablished safety and efficacy.

    Product
    Rhino 69 Extreme 50000 packaged in 1 capsule per blister pack, Distributed by AMA Wholesale Inc. Chino Hills, CA, 91709-2618, UPC Code: 718122071128
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1480-2018·2018-05-30

    FDA Recalls Nature's Only Choice B17 Apricot Extract Dietary Supplement

    Nature's Only Choice is recalling B17 Bitter Raw Apricot Extract Amygdalin dietary supplements because the product is considered an unapproved new drug.

    Product
    Nature's Only Choice B17 BITTER RAW APRICOT EXTRACT AMYGDALIN Dietary Supplement 100 Capsules
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0835-2018·2018-05-30

    Ideaz Recalls Screamin' Menthol Pain Gel Due to Benzene Levels

    Ideaz Llc is recalling Screamin' Menthol Pain Relieving Gel because it contains benzene levels exceeding FDA limits.

    Product
    screamin' menthol (menthol) Pain Relieving Gel, 4%, packaged in a) 2 OZ (57g) tubes, UPC 7 50263 80062 5; b) 5 oz. (141g) tubes, UPC 7 50263 80006 9; and c) 16 oz. (454g) bottles, UPC 7 50263 80066 3; MFD FOR: Toast Products, 400 Sproul Street, Pittsburgh, PA 15136; NDC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0834-2018·2018-05-30

    Ideaz Recalls Screamin' Hot Pain Gel Due to Benzene Levels

    Ideaz LLC is recalling Screamin' Hot Pain Relieving Gel because it was manufactured with benzene levels exceeding FDA limits.

    Product
    screamin' hot (capsaicin) Pain Relieving Gel, 0.03%, packaged in a) 2 OZ (57g) tubes, UPC 7 50263 80072 4; b) 5 oz. (141g) tubes, UPC 7 50263 80007 6; and c) 16 oz. (454g) bottles, UPC 7 50263 80076 2; MFD FOR: Toast Products, 400 Sproul Street, Pittsburgh, PA 15136; NDC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0827-2018·2018-05-30

    Fresenius Recalls 0.9% Sodium Chloride Injection Due to Sterility Concerns

    Fresenius Medical Care is recalling 25,356 bags of 0.9% Sodium Chloride Injection due to a lack of assurance of sterility.

    Product
    0.9% Sodium Chloride Injection, USP, 1000 mL, Rx Only, Fresenius Medical Care North America, Waltham, MA 02451, NDC 49230-0300-10.
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1901-2018·2018-05-30

    LivaNova Recalls Sorin Stockert Heater-Cooler Systems Due to Suspected Microbial Contamination

    LivaNova USA is recalling 2,408 Sorin Stockert Heater-Cooler System 3T units because they are suspected of microbial contamination and may contain visible biofilm.

    Product
    Sorin Stockert Heater-Cooler System 3T, a) Item #: 16-02-81, 240 v/60 Hz; b) Item #: 16-02-82, 208 v/60 Hz; c) Item #: 16-02-85, 120 v/60 Hz
    Category
    Medical Device
    Distribution
    44 states
  • SevereFDA (Food)·F-1490-2018·2018-05-30

    Shawnee Milling Recalls Self-Rising Flour for Metal Fragment Risk

    Shawnee Milling Company is recalling 1,350 bags of self-rising flour in four states due to potential metal fragments.

    Product
    Hilltop Hearth Self-Rising Flour, Katy s Kitchen Self-Rising Flour, Springwell A1 Flour all packaged in 50 pound paper bags
    Category
    Food
    Distribution
    4 states