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 deaths or serious injuries are reported, 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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13726–13750 of 31490

  • SevereNHTSA·24V653000·2024-05-09

    RAM 1500 Models Recalled for Anti-Lock Brake Software Malfunction

    Chrysler is recalling certain 2019, 2021-2024 RAM 1500 vehicles because a software malfunction in the ABS control module may disable the electronic stability control system, increasing crash risk.

    Product
    RAM — 2024 RAM 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V726000·2024-05-09

    Keystone Travel Trailers Recalled for Loose Hydraulic Leveling Foot Pads

    Keystone is recalling certain 2020-2023 travel trailers because hydraulic leveling leg foot pads may become loose and separate from the vehicle. A separated foot pad can become a road hazard, increasing the risk of a crash.

    Product
    KEYSTONE — 2020 KEYSTONE FUZION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24230·2024-05-09

    Zegoo Children's Nightgowns Recalled for Flammability Standard Violation

    About 14,000 Zegoo Children's Nightgowns sold on Amazon.com violate federal flammability standards for children's sleepwear, posing a burn injury risk. No injuries have been reported.

    Product
    Zegoo Children's Nightgowns
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V654000·2024-05-09

    2024 Porsche Taycan Headlight Control Software Defect Recall

    Porsche is recalling 954 model year 2024 Taycan vehicles due to incorrect headlight control module software that may prevent parking lights from functioning when turn signals are activated, potentially reducing visibility and increasing crash risk.

    Product
    PORSCHE — 2024 PORSCHE TAYCAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24226·2024-05-09

    ZLINE Built-In Electric Wall Ovens Recalled for Impact Injury Hazard

    ZLINE Kitchen and Bath is recalling about 5,000 built-in electric wall ovens because the oven door hinge can dislodge and release the spring, which may break through the door trim and cause impact injuries. Consumers should stop using the recalled ovens immediately.

    Product
    ZLINE Wall Ovens
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V727000·2024-05-09

    2022 Lucid Air: Tow Eye Bracket Detachment Risk During Towing

    Lucid is recalling certain 2022 Air vehicles where the front tow eye bracket may be inadequately attached to the subframe and can detach during towing. This could separate the vehicle from the tow truck, increasing crash risk.

    Product
    LUCID — 2022 LUCID AIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24228·2024-05-09

    Arctic Cat 2024 Catalyst 600 Snowmobiles Recalled for Crash Hazard

    Textron Specialized Vehicles is recalling about 2,670 Arctic Cat Model Year 2024 Catalyst 600 snowmobiles because steering caps can crack and cause handlebars to become unstable, posing a crash hazard. No injuries have been reported.

    Product
    Arctic Cat Model Year 2024 Catalyst 600 snowmobiles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V652000·2024-05-09

    Instrument Panel Cluster May Fail in Jeep Wrangler Vehicles

    Jeep is recalling certain 2018-2024 Wrangler and 2020-2024 Gladiator vehicles because the instrument panel cluster may fail due to an internal short circuit, preventing drivers from seeing the speedometer and warning lights.

    Product
    JEEP — 2020 JEEP WRANGLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24232·2024-05-09

    Korimefa Multi-Purpose Bike Helmets Recalled for Head Injury Risk

    Korimefa Multi-Purpose Bike Helmets do not meet federal safety standards for positional stability and may fail to protect in a crash. Approximately 60 units were sold online through Amazon from April 2022 through November 2022.

    Product
    Korimefa Multi-Purpose Bike Helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V724000·2024-05-09

    Chevrolet Equinox and GMC Terrain driver seat frame bolt defect

    General Motors is recalling certain 2022-2023 Chevrolet Equinox and 2022 GMC Terrain vehicles due to a potential issue with the driver's seat frame. The seat may not properly restrain an occupant in a crash.

    Product
    CHEVROLET — 2022 CHEVROLET EQUINOX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24233·2024-05-09

    SIORO Children's Robes Recall Due to Burn Hazard and Flammability Violation

    SIORO-branded children's robes violate federal flammability standards for children's sleepwear, posing a risk of burn injuries. About 5,000 units were sold on Amazon from November 2021 through July 2023.

    Product
    SIORO Children's Robes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24229·2024-05-09

    Textron Prowler Pro and Tracker UTVs Recalled for Fire Hazard

    Textron Specialized Vehicles is recalling about 10,300 Prowler Pro and Tracker 800SX utility vehicles due to a defective fuel tank cap that can leak fuel and pose a fire hazard. No injuries have been reported.

    Product
    Prowler Pro and Tracker 800SX Utility Vehicles (UTVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24227·2024-05-09

    Cotton On USA Recalls Toy Pinwheels Due to Choking Hazard

    Cotton On USA is recalling about 8,500 toy pinwheels because the fastener cap can come loose and detach, posing a choking hazard to young children. One child has swallowed a detached cap.

    Product
    Toy Pinwheels
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·24231·2024-05-09

    Spin Swivel Chairs Recalled Due to Fall Hazard

    Spin Swivel Chairs sold online at article.com from July 2021 through June 2023 are being recalled because the swivel chair's base can break, posing a fall hazard. No injuries have been reported.

    Product
    Spin Swivel Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1692-2024·2024-05-08

    Left ventricular assist system implant kit recalled for potential inflow cannula seal leak

    Thoratec HeartMate 3 left ventricular assist system implant kits may develop a leak at the seal interface between the inflow cannula and titanium apical cuff, potentially compromising device function.

    Product
    Thoratec HeartMate 3, LVAS Implant Kit, REF:106524US, Sterile EO, RxOnly
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1693-2024·2024-05-08

    Thoratec HeartMate 3 Left Ventricle Assist System Recalled for Seal Leak

    Thoratec recalls HeartMate 3 left ventricle assist systems due to potential leaks at the seal interface. The FDA Class I recall affects 659 implanted devices worldwide.

    Product
    Thoratec HeartMate 3, LVAS Implant Kit, REF:106524INT, Sterile EO, RxOnly
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1238-2024·2024-05-08

    King Kullen Broccoli Cutlets Recalled for Undeclared Wheat and Sesame

    King Kullen Broccoli Cutlets with Breadcrumbs and Parmesan are being recalled because they contain undeclared wheat and sesame, which can cause allergic reactions in sensitive consumers.

    Product
    King Kullen Broccoli Cutlets with Breadcrumbs and Parmesan; 20oz; oven safe tin package with a clear dome top marked with a UPC Code 0 8531610145 0
    Category
    Food
    Distribution
    0 states
  • SevereNHTSA·23V588000·2024-05-08

    2023 Honda Accord and CR-V Hybrid transmission defect can cause power loss

    Honda is recalling certain 2023 Accord Hybrid and CR-V Hybrid vehicles because the electronic continuously variable transmission (e-CVT) may have been improperly manufactured, potentially resulting in loss of drive power and increased crash risk.

    Product
    HONDA — 2023 HONDA ACCORD HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1244-2024·2024-05-08

    International Bread Pita Chips Recalled for Undeclared Wheat Allergen

    International Bread Pita Chips are recalled because the label declares flour as an ingredient but does not identify wheat as a sub-ingredient. This poses a risk to consumers with wheat allergies.

    Product
    International Bread Pita Chips Retail Clamshell Container: 10oz., Bulk bag: 10lbs. UPC: Plain Baked Pita Chips: 6 81942 22110 6
    Category
    Food
    Distribution
    1 state
  • HighFDA (Drugs)·D-0476-2024·2024-05-08

    FDA Issues Nationwide Recall of Subpotent Ophthalmic Eye Drops

    The FDA is recalling 3,320 bottles of compounded ophthalmic solution due to subpotency. The affected product does not contain adequate amounts of active medication.

    Product
    Prednisolone Sodium Phosphate-Moxifloxacin-Bromfenac Sterile Ophthalmic Solution 1%, 0.5%, 0.075%, 8mL, Compounded By: Imprimis NJOF, LLC. 1705 Route 46 West, Unit 6B Ledgewood, NJ 07852, NDC 71384-340-08
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1737-2024·2024-05-08

    Jackson-Pratt 3-Spring Reservoir Kit Recalled Due to Non-Sterile Shipment

    Cardinal Health is recalling Jackson-Pratt 3-Spring Reservoir Kits after shipping specific lots before sterilization. The affected devices pose an infection risk if used without proper sterilization.

    Product
    Jackson-Pratt 3-Spring Reservoir Kit with PVC Round Drain, 400mL, 15Fr., REF SU130-403D
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1748-2024·2024-05-08

    Radiation Therapy Planning System May Calculate Skin Surface Distance Incorrectly

    RayStation radiation therapy planning software versions 11.0.0.951, 11.0.1.29, 11.0.3.116, and 11.0.4.15 may calculate skin surface distance (SSD) values incorrectly, potentially affecting dose calculations. Affected software has been distributed worldwide.

    Product
    RayStation 11.0.0.951, 11.0.1.29, 11.0.3.116 & 11.0.4.15. Radiation Therapy Treatment Planning System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1741-2024·2024-05-08

    RayStation 7.0.0.19 radiation therapy planning software recalled for dose calculation error

    RayStation 7.0.0.19, a radiation therapy treatment planning system, is being recalled due to potential source-to-surface distance (SSD) calculation errors that could affect radiation dose accuracy. The recall affects 14 units distributed worldwide.

    Product
    RayStation 7.0.0.19. Radiation Therapy Treatment Planning System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1738-2024·2024-05-08

    Jackson-Pratt Drainage Kits Shipped Unsterilized in Voluntary Removal

    Cardinal Health is voluntarily removing Jackson-Pratt drainage kits (Lot 210751D6) that were shipped without sterilization. The unsterilized devices pose an infection risk if used in patient care.

    Product
    Jackson-Pratt Universal Connector PVC Tubing Anti Reflux Transparent Y, REF SU130-4601
    Category
    Medical Device
    Distribution
    Distributed nationwide