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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3376–3400 of 36538

  • SevereNHTSA·24V740000·2024-10-03

    Terex Recalls 2023-2024 TL and TM Series Vehicles for Hydraulic Defect

    Terex is recalling 2023-2024 TL and TM series vehicles because a weak weld on the jib extension hydraulic cylinder rod may fail, increasing injury risk.

    Product
    TEREX — TEREX TM-SERIES, TL-SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V742000·2024-10-03

    2025 Winnebago Navion Motorhomes Recalled for Seat Belt Retractor Damage

    Winnebago Industries is recalling 2025 Navion and View motorhomes because a screw may damage the seat belt retractor. A damaged retractor may not secure occupants properly, increasing the risk of crash-related injury.

    Product
    WINNEBAGO — WINNEBAGO VIEW, NAVION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3091-2024·2024-10-02

    Smiths Medical Recalls paraPAC 300 Ventilator Kits Due to Connector Issue

    Smiths Medical is recalling 3,182 paraPAC 300 ventilator kits because the patient outlet connector may loosen or detach, impacting active ventilation.

    Product
    paraPAC 300 ventilator kit without internal PEEP and CPAP, Item Number P300N
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-3137-2024·2024-10-02

    CARDIOSAVE RESCUE intra-aortic balloon pump software correction for hemodynamic instability

    Datascope Corp. is issuing a software correction for CARDIOSAVE RESCUE intra-aortic balloon pump devices to address risks of hemodynamic instability and failure to properly transmit clinical data worldwide.

    Product
    CARDIOSAVE RESCUE INTRA-AORTIC BALLOON PUMP (IABP). Electromechanical system used to inflate and deflate intra-aortic balloons.
    Category
    Medical Device
    Distribution
    0 states
  • SevereNHTSA·24V750000·2024-10-02

    School buses recalled for brake caliper mounting bolt defect

    Navistar is recalling 2024-2025 IC Bus school buses because brake caliper mounting bolts may not be properly tightened, allowing the brake caliper to detach and cause loss of braking ability. Owner notification was sent in November 2024.

    Product
    IC BUS — IC BUS CESB, EVSB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V739000·2024-10-02

    2024 BMW i7 M70 Integrated Brake Module Malfunction Affects Stopping and Control

    BMW is recalling certain 2024 i7 M70 and related models because the integrated brake module may malfunction, potentially reducing braking power and vehicle control. Dealers will replace the module at no cost.

    Product
    BMW — BMW 760I XDRIVE, 740I, 530I XDRIVE, I5 EDRIVE40
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3090-2024·2024-10-02

    ParaPAC Plus 310 ventilator connector may detach and stop ventilation

    Smiths Medical is recalling paraPAC Plus 310 ventilators because the patient outlet connector may loosen or detach, potentially interrupting ventilation. Approximately 11,244 units worldwide are affected.

    Product
    paraPAC plus 310 ventilator kit with internal PEEP and CPAP, Item Number P310N
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-3135-2024·2024-10-02

    CARDIOSAVE Rescue IABP software defect poses hemodynamic instability risk

    Datascope CARDIOSAVE Rescue IABP devices have a software defect that risks hemodynamic instability and clinical data transmission failure. A software correction is available.

    Product
    CARDIOSAVE RESCUE INTRA-AORTIC BALLOON PUMP (IABP). Electromechanical system used to inflate and deflate intra-aortic balloons.
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-3292-2024·2024-10-02

    Boston Scientific Recalls Agile Esophageal Stent Systems Due to Catheter Tip Detachment

    Boston Scientific is recalling Agile Esophageal Over the Wire Stent Systems because the delivery catheter tip may detach. The recall affects 19 units distributed worldwide.

    Product
    AGILE ESO OTW FC 23MM X 15.0CM IN 18.5 F-Agile Esophageal Partially Covered (PC) and Fully Covered (FC) OTW Stent System is intended for maintaining esophageal luminal patency in esophageal strictures caused by intrinsic and/or extrinsic malignant tumors, and occlusion of concu
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3153-2024·2024-10-02

    Ivenix Infusion Pump Software Recalled for Potential Malfunctions

    Fresenius Kabi is recalling Ivenix Infusion System software (Version 5.9.1 and prior) due to anomalies that can cause pump malfunctions, alarms, or unresponsive screens while delivering medication, risking serious patient harm.

    Product
    Ivenix Infusion System (IIS), LVP Software; LVP-SW-0004, Software Version 5.9.1 and prior. Infusion pump software for infusion management system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3134-2024·2024-10-02

    Cardiosave hybrid IABP software defect poses hemodynamic instability and data loss risk

    Datascope's Cardiosave Hybrid IABP devices carry a risk of hemodynamic instability and clinical data transmission failure due to a software defect. Datascope has developed a software correction (Revision D.00) to mitigate this risk.

    Product
    CARDIOSAVE HYBRID INTRA-AORTIC BALLOON PUMP (IABP). Electromechanical system used to inflate and deflate intra-aortic balloons.
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-3289-2024·2024-10-02

    Boston Scientific Recalls Agile Esophageal Stent Systems Due to Catheter Tip Detachment

    Boston Scientific is recalling Agile Esophageal Stent Systems because the delivery catheter tip may detach. The recall affects 17 units distributed worldwide.

    Product
    AGILE ESO OTW PC 23MM X 12.0CM IN 18.5 F-Agile Esophageal Partially Covered (PC) and Fully Covered (FC) OTW Stent System is intended for maintaining esophageal luminal patency in esophageal strictures caused by intrinsic and/or extrinsic malignant tumors, and occlusion of concu
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V738000·2024-10-02

    GM Recalls 2024-2025 Chevrolet Silverado HD Trucks for Inactive Air Bags

    General Motors is recalling certain 2024-2025 Chevrolet Silverado HD trucks because the air bag module may not have been activated, preventing deployment in a crash.

    Product
    CHEVROLET — CHEVROLET SILVERADO 5500, SILVERADO 6500, SILVERADO 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V732000·2024-10-01

    2021-2024 Porsche Taycan battery short circuit fire risk

    Porsche is recalling 2021-2024 Taycan vehicles due to high-voltage battery short circuits that increase fire risk. Dealers will install diagnostic software and replace batteries as needed, advising owners to charge only to 80% capacity until repairs are completed.

    Product
    PORSCHE — PORSCHE TAYCAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V727000·2024-09-30

    Nova Bus control unit software crash can cut drive power

    Nova Bus is recalling certain 2022-2023 LFS buses because a software error may cause the Vehicle Control Unit to crash, disconnecting the high voltage batteries and causing a loss of drive power.

    Product
    NOVA BUS — NOVA BUS LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V723000·2024-09-27

    Volkswagen Atlas brake master cylinder can block fluid port losing braking

    Volkswagen is recalling certain 2024 Atlas and Atlas Cross Sport vehicles because the brake master cylinder may have an incorrect secondary piston spring retainer that can block the brake fluid port.

    Product
    VOLKSWAGEN — VOLKSWAGEN ATLAS CROSS SPORT, ATLAS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·027-2024·2024-09-27

    Pork Dynasty Recalls Fried Pork Skin Products for Undeclared Soy Allergen

    Pork Dynasty Inc. is recalling approximately 469 pounds of ready-to-eat fried pork skin products because they contain soy, a known allergen, that is not declared on the label.

    Product
    Pork Dynasty, Inc. — Pork Dynasty Inc. Recalls Ready-to-Eat Fried Pork Skin Products Due to Misbranding and Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V720000·2024-09-27

    Jeep 4XE high voltage batteries can fail and catch fire

    Chrysler is recalling certain 2020-2024 Wrangler 4XE and 2022-2024 Grand Cherokee 4XE vehicles because the high voltage battery may fail internally and cause a fire while parked or driving.

    Product
    JEEP — JEEP GRAND CHEROKEE 4XE, WRANGLER 4XE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V724000·2024-09-27

    Mercedes-Benz Recalls GLE 350 and GLE 450 for Air Bag Wiring Defect

    Mercedes-Benz is recalling 2021-2022 GLE 350 and GLE 450 vehicles because an incorrectly routed wiring harness may prevent front air bags from deploying properly.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE 350, GLE 450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24E080000·2024-09-27

    Chrysler Recalls Mopar Hybrid Service Kit Battery Packs Due to Fire Risk

    Chrysler is recalling specific Mopar Hybrid Service Kit Battery Packs because they may fail internally and cause a fire. Owners should park outside and not recharge until repaired.

    Product
    ELECTRICAL SYSTEM:PROPULSION SYSTEM:TRACTION BATTERY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V717000·2024-09-26

    Brinkley Model Z safety chains are underrated for the weight rating

    Brinkley RV is recalling certain 2025 Model Z travel trailers because the installed safety chains are underrated for the Gross Vehicle Weight Rating. 40 units are affected.

    Product
    BRINKLEY RV — BRINKLEY RV MODEL Z
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·24377·2024-09-26

    John Deere Compact Utility Tractors Recalled for Brake Failure Hazard

    Deere & Company is recalling about 147,900 John Deere 1023E, 1025R, and 2025R Compact Utility Tractors because the front bell crank in the brake linkage can fail, causing loss of braking and crash risk. Four failures have been reported, including one hospitalization and two impact injuries.

    Product
    John Deere 1023E, 1025R, and 2025R Compact Utility Tractors
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-3084-2024·2024-09-25

    Baxter pharmaceutical compounding inlets recalled for particulate matter contamination

    Baxter is recalling EXACTAMIX compounding device inlets due to particulate matter observed in sterile fluid pathways before use. Approximately 5.8 million units affected worldwide.

    Product
    Baxter EXACTAMIX Inlet, Vented, Micro-Volume Inlet, REF H938175, for use in a pharmaceutical compounding device
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Food)·F-1816-2024·2024-09-25

    Supreme Guacamole and Pico Products Recalled for Possible Listeria Contamination

    GBC Food Services is recalling Supreme brand guacamole and pico/guacamole products distributed in Indiana due to possible contamination with Listeria monocytogenes.

    Product
    Supreme Guacamole Chunky Mild 8-50053-68588 17 OZ Supreme Guacamole Chunky Medium 8-50053-68589 17 OZ Supreme Pico/Guacamole 8-50054-89443 16 OZ Supreme Pico/Guacamole
    Category
    Food
    Distribution
    1 state