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

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All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

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

Clear filters

13476–13500 of 89746

  • HighFDA (Devices)·Z-1528-2024·2024-04-24

    Peel-Away Introducer medical devices recalled for low packaging seal strength

    Cook Incorporated is recalling 55 Peel-Away Introducers due to packaging with low seal strength that may compromise device sterility.

    Product
    Peel-Away Introducer - Intended for the percutaneous introduction of balloon, electrode and closed or non-tapered end catheters into central and peripheral vasculature, and for nonvascular use. REFERENCE PART NUMBER (RPN)/ ORDER NUMBER (GPN): 1)PLVW-7.0-35 G00925…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1578-2024·2024-04-24

    Magnetic Resonance System patient support table floor plate installation defect

    Philips has recalled Intera 1.5T Achieva Nova-Dual MRI systems due to incorrect installation of the patient support table floor plate. The recall affects 20 units distributed worldwide.

    Product
    Intera 1.5T Achieva Nova-Dual, Magnetic Resonance System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1591-2024·2024-04-24

    Conformis Identity Imprint PS Tibial Tray Size 4 Packaging Error

    Conformis is recalling Identity Imprint PS Tibial Tray Size 4 implants due to a packaging error where Size 5 components were placed in Size 4 boxes with incorrect lot numbers.

    Product
    Identity Imprint PS Tibial Tray Size 4: Lot 540287
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1598-2024·2024-04-24

    Siemens Artis X-ray systems cooling malfunction may halt procedures

    Siemens Artis interventional X-ray systems may fail to cool the X-ray tube adequately, causing system shutdown and potentially requiring cancellation of clinical imaging procedures. The recall affects 583 units distributed nationwide.

    Product
    Siemens Artis Models: Interventional Fluoroscopic X-Ray Systems-Models: Artis zee floor- 10094135 Artis zee ceiling- 10094137 Artis zee multi-purpose- 10094139 Artis zee biplane- 10094141 Artis zeego- 10280959 Artis Q floor- 10848280 Artis Q ceiling- 10848281 Artis Q…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1175-2024·2024-04-24

    Plate Set Recalled for Potential Excess Leachable Lead

    Canadian Art Prints is recalling Tranquility & Teachings plate sets that may exceed FDA guidance levels for leachable lead. The recall affects 83 boxes distributed across 14 U.S. states.

    Product
    Tranquility & Teachings William Monague plate set, brand Indigenous Collection by CAP. Each box consists of two plates, each plate is 7.5inch. Stock code PLT015, UPC 772665860151. Tranquility plate #1 artwork is observed with a lakeside landscape at night in blues and greens…
    Category
    Consumer Product
    Distribution
    15 states
  • HighFDA (Devices)·Z-1562-2024·2024-04-24

    MRI Patient Support Table Floor Plate May Be Incorrectly Installed

    Philips GYROSCAN T5-NT MRI systems may have an incorrectly installed patient support floor plate. Affected units should be inspected to ensure proper installation.

    Product
    GYROSCAN T5-NT, Magnetic Resonance System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1560-2024·2024-04-24

    Philips GYROSCAN T10-NT MRI Systems Patient Support Table Floor Plate Installation Issue

    Philips North America is recalling GYROSCAN T10-NT MRI systems due to potential incorrect installation of the patient support table floor plate. Affected units should be verified for proper installation.

    Product
    GYROSCAN T10-NT, Magnetic Resonance System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1526-2024·2024-04-24

    Trocar Needle Recall Due to Packaging Seal Strength Defect

    Cook Incorporated recalled 55 Trocar Needles (Lot 15786588) due to packaging that may not meet peel strength specifications, potentially compromising device sterility. Units were distributed nationwide and internationally.

    Product
    Trocar Needle - Used for dilating puncture sites or catheter tracts for percutaneous placement of devices for vascular and non-vascular applications such as in the venous, arterial, biliary and renal system REFERENCE PART NUMBER (RPN): DTN-18-20.0 ORDER NUMBER (GPN)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1544-2024·2024-04-24

    Neria Soft Infusion Sets recalled due to incorrect instruction manual

    Unomedical A/S is recalling 10,770 units of Neria Soft Infusion Sets because certain lots were shipped with incorrect instructions for use. The wrong instruction manual for Rest of World markets was included instead of the FDA-approved US version.

    Product
    Neria Soft Infusion Set, Product Code 507302, intravascular administration set
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1552-2024·2024-04-24

    Philips Achieva 1.5T MRI System: Patient Support Table Floor Plate Installation Issue

    Philips is recalling 69 units of the Achieva 1.5T Initial MRI system due to potential issues with the patient support table floor plate installation, which may affect patient safety during imaging.

    Product
    Achieva 1.5T Initial, Magnetic Resonance System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1550-2024·2024-04-24

    Philips Achieva 1.5T MRI Systems Recalled Due to Incorrect Support Table Installation

    Philips is recalling 1,921 Achieva 1.5T MRI systems worldwide because the patient support table floor plate may be incorrectly installed. Healthcare facilities should verify proper installation.

    Product
    Achieva 1.5T, Magnetic Resonance System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1549-2024·2024-04-24

    Siemens Atellica Lab Analyzers Risk Falsely Elevated Cholesterol Results

    Siemens Atellica CH and CI analyzers may produce falsely elevated cholesterol and lipid test results (2–16% high) after iron tests. This affects clinical calibration, quality control checks, and patient test results.

    Product
    Atellica CH Iron3 - IVD use in the quantitative measurement of iron in human serum and plasma (lithium heparin and sodium heparin) using the Atellica¿ CI Analyzer and Atellica¿ CH Analyzer Siemens Material Number (SMN): 11537211
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1592-2024·2024-04-24

    Fetal Membrane Rupture Test Kits Recalled for False Positive Results

    Actim PROM dipstik fetal membrane rupture test kits are recalled because personal lubricants can interfere with the test, producing false positive results.

    Product
    Actim PROM dipstik, REF 30831ETUS; qualitative immunoassay rapid test for rupture of fetal membrane
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V287000·2024-04-23

    Kia Sorento power steering wiring harnesses may be incorrectly assembled

    Kia is recalling certain 2024 Sorento vehicles because the motor driven power steering wiring harness may be incorrectly assembled, which can result in a loss of power steering assist.

    Product
    KIA — KIA SORENTO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V285000·2024-04-23

    Winnebago towable cooktop circuit boards may fail and overheat

    Winnebago Towable is recalling certain 2022-2024 travel trailers because the LED backlight circuit board in the cooktop range may fail and overheat. 13,117 units affected.

    Product
    WINNEBAGO — WINNEBAGO MINNIE, VOYAGE, MICRO MINNIE, HIKE200
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V286000·2024-04-23

    Alliance RV freshwater tanks may be installed incorrectly and detach

    Alliance RV is recalling certain 2022 Paradigm 295MK and Avenue 32RLS fifth wheels because the freshwater tank may be installed incorrectly and detach from the vehicle.

    Product
    ALLIANCE RV — ALLIANCE RV PARADIGM, AVENUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24T004000·2024-04-23

    Rocky Mountain ATV/MC Recalls Tusk 2Track Adventure Motorcycle Tires

    Rocky Mountain ATV/MC is recalling Tusk 2Track Adventure rear motorcycle tires because the tread layer was improperly cured, which can cause tread detachment and loss of vehicle control.

    Product
    TIRES:TREAD/BELT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-04202024-001·2024-04-20

    Ground Beef Products Subject to Public Health Alert for E. Coli O157:H7

    USDA FSIS issued a public health alert for Greater Omaha Packing Co. ground beef products due to possible E. coli O157:H7 contamination. Consumers should not consume these products.

    Product
    Greater Omaha Packing Co., Inc. — FSIS Issues Public Health Alert for Ground Beef Products Due to Possible E. Coli O157:H7 Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V281000·2024-04-19

    REV Ambulance Recalls 76 Vehicles Due to Electrical Fire Risk

    REV Ambulance Group Orlando is recalling 76 ambulances from 2019-2024 because a firmware defect may cause electrical circuits to overheat and increase the risk of fire.

    Product
    REV AMBULANCE — REV AMBULANCE TYPE IX, TYPE I, TYPE III
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V284000·2024-04-19

    2024 Tesla Model 3 Side Air Bag Module Missing Deflector

    Tesla is recalling one 2024 Model 3 vehicle. The driver seat side air bag module was assembled without a deflector, which may cause improper deployment and increase the risk of injury during a crash.

    Product
    TESLA — TESLA MODEL 3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V283000·2024-04-19

    2024 Hyundai IONIQ 6 Differential Gear Drive Unit Recall

    Hyundai is recalling certain 2024 IONIQ 6 vehicles because differential gear bolts in the gear drive unit may not be tightened properly, risking loss of drive power or differential lockup that could increase crash risk.

    Product
    HYUNDAI — HYUNDAI IONIQ 6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V279000·2024-04-19

    REV Recalls Fleetwood and Holiday Rambler Motorhomes for Fire Risk

    REV is recalling 2022-2024 Fleetwood Discovery and Holiday Rambler Endeavor motorhomes because inadequate fuse protection on the water pump harness may cause a fire.

    Product
    FLEETWOOD — FLEETWOOD, HOLIDAY RAMBLER DISCOVERY, ENDEAVOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V282000·2024-04-19

    Genesis G90 fuel pump failure may cause loss of drive power

    Hyundai is recalling certain 2022–2023 Genesis GV70, GV80, G80, and G90 vehicles because the fuel pump may fail, resulting in loss of drive power and increased crash risk.

    Product
    GENESIS — GENESIS GV80, G80, GV70, G90
    Category
    Vehicle
    Distribution
    Distributed nationwide