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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10476–10500 of 89670

  • HighFDA (Devices)·Z-0037-2025·2024-10-16

    FDA Recalls EPIONE Device Due to Internal Component Corrosion

    Quantum Surgical recalls 2 units of the EPIONE device v1.0.2 because rust has developed on the central axis component of the Needle Guide product. These units were distributed in Florida.

    Product
    The EPIONE device v1.0.2 is a user controlled, stereotactic accessory device intended to assist in the planning and manual advancement of one or more instruments, as well as in verification of instrument position during Computed Tomography (CT) guided percutaneous procedures. Du
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0055-2025·2024-10-16

    Enterprise Imaging XERO Viewer medical software reference line placement error

    Enterprise Imaging XERO Viewer incorrectly displays reference lines on medical images due to a software defect affecting images with non-square pixel spacing. The misplaced reference lines may lead to diagnostic errors.

    Product
    Enterprise Imaging XERO Viewer- software application used for reference and diagnostic viewing of multispecialty medical imaging and non-imaging data . Enterprise Imaging XERO Viewer 8.0.0, 8.0.1, 8.1, 8.1.1, 8.1.2, 8.1.3,8.1.4, 8.2.0.000, 8.2.1.000, 8.2.2.000, 8.3.0.000, 8.3.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0025-2025·2024-10-16

    Coca-Cola recalls Minute Maid Zero Sugar Lemonade due to mislabeling

    COCA COLA Consolidated LLC recalls Minute Maid Zero Sugar Lemonade cartons sold in Indiana, Kentucky, and Ohio. Regular Minute Maid Lemonade cans were incorrectly placed in Zero Sugar packaging.

    Product
    Minute Maid Zero Sugar Lemonade 12 cans carton UPC 0 25000 12115 9 CANNED UNDER THE AUTHORITY OF THE COCA-COLA COMPANY, ATLANTA, GA
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-0022-2025·2024-10-16

    FastPack TSH Calibrator Kit Recalled Due to Incorrect Barcode

    Qualigen Inc is recalling the FastPack TSH Calibrator Kit due to an incorrect barcode linked to incorrect information. The barcode defect may allow successful system calibration, but TSH test results obtained could be higher than expected.

    Product
    FastPack TSH Calibrator Kit, REF: 25000024, For use in conjunction with the FastPack IP TSH Immunoassay and FastPack IP System Analyzer
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Devices)·Z-0054-2025·2024-10-16

    MEDIHONEY Dressing Applicator Pouch Recalled for Sterility Concerns

    Integra LifeSciences recalls MEDIHONEY Dressing applicator pouches due to potential pinholes that may compromise sterility. The recall affects approximately 120,124 units distributed across 36 US states and internationally.

    Product
    MEDIHONEY Dressing with Active Leptospermum Honey Wound and Burn Dressing W/APPLICATOR, 1.5oz tube (Model Number 31515) and 3.5oz tube (Model Number 31535)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0020-2025·2024-10-16

    Philips IntelliVue Patient Monitor Software Configuration Disables Enhanced ECG Alarms

    Philips patient monitors with Option CP2 software version P.01.01 were factory-configured incorrectly, leaving enhanced arrhythmia detection alarms disabled. Affected devices will not trigger yellow alarms for enhanced arrhythmia detection.

    Product
    IntelliVue Patient Monitor MX400/MX450/MX500/MX550 with software version P.01.01 and ordered with Option CP2 are affected as follows: 1) IntelliVue MX400 866060; 2) IntelliVue MX450 866062; 3) IntelliVue MX500 866064; 4) IntelliVue MX550 866066 Indica
    Category
    Medical Device
    Distribution
    0 states
  • HighNHTSA·24V768000·2024-10-16

    Multiquip Recalls Trailers Due to Frame Weld Cracking Risk

    Multiquip is recalling specific 2010-2016 trailers because frame welds may crack or break, reducing stability and increasing crash risk.

    Product
    MULTIQUIP — MULTIQUIP TRLR-55164, TRLR-57615, TRLR-55348
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0039-2025·2024-10-16

    GE Healthcare Centricity Universal Viewer may fail to display latest diagnostic report

    GE Healthcare Centricity Universal Viewer Zero Footprint Client version 6.0 SP11.x may fail to show the latest diagnostic report by default when a study contains multiple DICOM structured reports in different series.

    Product
    GE Healthcare Centricity Universal Viewer Zero Footprint Client, Model/Catalog/Code Numbers: a)¿¿¿¿¿ 2089507-120; b)¿¿¿¿ 2089507-129; c)¿¿¿¿¿ 2089507-131; d)¿¿¿¿ 2089507-135; e)¿¿¿¿ 2089507-136; f)¿¿¿¿¿¿ 2089507-140; g)¿¿¿¿¿ 2089507-144; h)¿¿¿¿ 2089507-145; i)¿
    Category
    Medical Device
    Distribution
    0 states
  • HighNHTSA·24V764000·2024-10-15

    2018–2022 BMW X3 rear cargo rail attachment defect recall

    BMW is recalling 2018–2022 X3 vehicles because rear cargo rail attachment bolts may become damaged in a rear crash, causing the rail to detach and increasing injury risk. Dealers will replace the bolts free of charge.

    Product
    BMW — BMW X3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V765000·2024-10-15

    Lamborghini Recalls 2024 Revuelto Vehicles Due to Wiper Rod Defect

    Lamborghini is recalling 2024 Revuelto vehicles because a wiper connecting rod may bend and separate, causing wiper failure and reduced visibility.

    Product
    LAMBORGHINI — LAMBORGHINI REVUELTO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V767000·2024-10-15

    2024 Toyota Sequoia Hybrid and Tundra Tire Sidewall Damage Recall

    Certain 2024 Toyota Sequoia Hybrid, Tundra, and Tundra Hybrid vehicles are recalled due to passenger-side front and rear tire sidewall damage that may cause sudden tire pressure loss and loss of vehicle control.

    Product
    TOYOTA — TOYOTA SEQUOIA HYBRID, TUNDRA HYBRID, TUNDRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V762000·2024-10-14

    Entegra Ethos and Jayco Swift Incorrect Tire Load Label Recall

    Jayco is recalling 2,044 units of 2021–2025 Entegra Ethos and Jayco Swift vehicles due to an incorrect Tire and Loading Information Label. The mislabeled tire load range could lead owners to select underrated replacement tires, increasing crash risk.

    Product
    JAYCO — JAYCO, ENTEGRA SWIFT LI, SWIFT, ETHOS LI, ETHOS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V763000·2024-10-14

    2025 Honda Civic fuel pump defect poses fire risk

    Honda is recalling certain 2023-2025 model year Civic vehicles because the high-pressure fuel pump may crack and leak fuel, increasing the risk of fire if an ignition source is present. Owners should contact Honda for free inspection and replacement.

    Product
    HONDA — HONDA ACCORD, CIVIC, CIVIC HYBRID, CR-V HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V759000·2024-10-11

    Blue Bird Transit Bus Recall for Illegible Emergency Exit Labels

    Blue Bird is recalling 2020-2024 All American and 2021-2024 Vision transit buses because emergency exit labels are too small to read, potentially delaying evacuation.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN TRANSIT BUS, VISION TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V760000·2024-10-11

    E-One Recalls Fire Trucks Due to Engine Crossmember Defect

    E-One is recalling 282 fire trucks because a broken engine crossmember can damage the cooling fan, causing an engine stall and increasing crash risk.

    Product
    E-ONE — E-ONE TYPHOON N, CYCLONE N, QUEST II, CYCLONE II
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V758000·2024-10-11

    Blue Bird Recalls School Buses for Illegible Emergency Exit Labels

    Blue Bird is recalling 2019-2024 Vision and All American school buses because emergency exit labels are too small to read, potentially delaying evacuation.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN, VISION, VISION SCHOOL BUS, ALL AMERICAN SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V761000·2024-10-11

    Hyundai Nexo Hydrogen Pressure Relief Device Defect Creates Fire Risk

    Hyundai is recalling 2019-2024 Nexo vehicles because the hydrogen pressure relief device may fail and leak, creating a fire risk. Owners are advised to park outside until the repair is complete.

    Product
    HYUNDAI — HYUNDAI NEXO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·25009·2024-10-10

    Fisher-Price Recalls 2.1 Million Snuga Infant Swings for Suffocation Risk

    Fisher-Price is recalling approximately 2.1 million Snuga Infant Swings due to suffocation hazard when the product is used for sleep or bedding is added. Five deaths have been reported between 2012 and 2022.

    Product
    All Models of Fisher-Price Snuga Swings
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·24E084000·2024-10-10

    Jaguar Recalls AJ20-P6 Engines Due to Oil Filter Housing Leak Risk

    Jaguar is recalling certain AJ20-P6 replacement engines because the oil filter housing may crack and leak, posing a fire and crash risk.

    Product
    ENGINE AND ENGINE COOLING:ENGINE:OIL/LUBRICATION recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24E085000·2024-10-10

    Land Rover Recalls AJ20-P6 Engines for Oil Filter Housing Cracks

    Land Rover is recalling AJ20-P6 replacement engines because the oil filter housing may crack and leak, increasing the risk of fire or road hazards.

    Product
    ENGINE AND ENGINE COOLING:ENGINE:OIL/LUBRICATION recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V756000·2024-10-10

    GM Recalls 2018-2019 Trucks for Air Bag Inflator Defect

    General Motors is recalling specific 2018-2019 Chevrolet and GMC trucks because side air bag inflators may rupture, posing an injury risk.

    Product
    GMC — GMC, CHEVROLET SIERRA 3500, SIERRA 2500, SILVERADO 3500, SILVERADO 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V754000·2024-10-10

    2020-2023 RAM 1500 Heated Rearview Mirror Glass May Detach

    Chrysler is recalling 2020-2023 RAM 1500 vehicles with heated trailer tow rearview mirrors. The mirror glass may detach, reducing driver visibility and increasing crash risk.

    Product
    RAM — RAM 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide