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

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All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

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

Clear filters

16176–16200 of 27500

  • SevereFDA (Devices)·Z-0989-2019·2019-03-13

    Maquet Flat Screen Monitor Holder Recalled for Grounding Non-Compliance

    Getinge US Sales LLC is recalling six Maquet XS Flat Screen Monitor Holders because they may not meet grounding requirements, posing a risk of electric shock.

    Product
    Maquet XS Flat Screen Monitor Holder, PWD70+DF HD R XS32 K3 SPE, Configuration Part Number ARD268400150A Product Usage: This product is designed to support one or two medical grade flat screen(s) alone or in association with surgical lights.
    Category
    Medical Device
    Distribution
    2 states
  • SevereFDA (Devices)·Z-0990-2019·2019-03-13

    Maquet XS Flat Screen Monitor Holder Recalled for Grounding Defect

    Getinge is recalling four Maquet XS Flat Screen Monitor Holders in Arizona and Texas because they may not meet grounding requirements, posing a risk of electric shock.

    Product
    Maquet XS Flat Screen Monitor Holder, SAT XS32 12 SPE, Configuration Part Number ARD2SAT00130A Product Usage: This product is designed to support one or two medical grade flat screen(s) alone or in association with surgical lights.
    Category
    Medical Device
    Distribution
    2 states
  • SevereFDA (Devices)·Z-0988-2019·2019-03-13

    Maquet XS Flat Screen Monitor Holder Recalled for Grounding Defect

    Getinge is recalling six Maquet XS Flat Screen Monitor Holders in Arizona and Texas because they may not meet grounding requirements, posing a risk of electric shock.

    Product
    Maquet XS Flat Screen Monitor Holder, PWD50+DF XS32 K3 SPE, Configuration Part Number ARD268400140A Product Usage: This product is designed to support one or two medical grade flat screen(s) alone or in association with surgical lights.
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-0975-2019·2019-03-13

    Draegar Medical Systems Recalls Omega Patient Monitor Software

    Draegar Medical Systems is recalling Omega patient monitor software due to cybersecurity vulnerabilities that may cause device reboots or loss of functionality.

    Product
    Omega Systems These devices are intended to be used in the environment where patient care is provided by Healthcare Professionals, i.e. Physicians, Nurses, and Technicians, who will determine when use of the device is indicated, based upon their professional assessment of the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0985-2019·2019-03-13

    Siemens Uroskop Omnia Max Fluoroscopic X-ray System Recall for Swivel Arm Defect

    Siemens is recalling 191 Uroskop Omnia Max fluoroscopic X-ray systems because the swivel arm holding the monitors may become dislodged from the carrying arm.

    Product
    Uroskop Omnia Max -fluoroscopic X-ray system Model # 10762473 Uroskop Omnia Max is a device intended to visualize anatomical structures by converting an X-ray pattern into a visible image.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0984-2019·2019-03-13

    Siemens Uroskop Omnia Fluoroscopic X-ray System Recalled for Monitor Arm Defect

    Siemens is recalling six Uroskop Omnia fluoroscopic X-ray systems because the swivel arm holding the monitors may become dislodged from the carrying arm.

    Product
    Uroskop Omnia -fluoroscopic X-ray system Model # 10094910 The Uroskop Omnia is a solid state detector fluoroscopic X-ray system, primarily for urological applications (functional x-ray diagnosis, endourology and minimal invasive urology/surgery).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0973-2019·2019-03-13

    Stryker Reprocessed Arthroscopic Shavers Recalled for Display and Function Errors

    Stryker is recalling 14,265 reprocessed arthroscopic shavers that may display incorrect settings or error messages, preventing proper use during surgery.

    Product
    Stryker Sustainability Solutions (SSS) reprocessed Arthroscopic Shavers Arthroscopic shavers can be used to abrade, cut and excise tissue and bone; remove loose fragments; and, shave away debris in arthroscopic surgeries, as well as surgeries of the jaw and sinuses. Intended…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0971-2019·2019-03-13

    Abbott Recalls Architect Magnesium Assay Due to Depressed Urine Results

    Abbott is recalling Architect Magnesium assays because urine tests may show falsely low results. The recall covers 24,995 units distributed in the US and four other countries.

    Product
    ARCHITECT MAGNESIUM, (a) REF 7D70-21, (b) 7D70-31 The Magnesium assay is used for the quantitation of magnesium in human serum, plasma, or urine.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0974-2019·2019-03-13

    Draeger Infinity Delta Patient Monitors Recalled for Cybersecurity Vulnerabilities

    Draeger Medical Systems is recalling Infinity Delta patient monitors due to cybersecurity vulnerabilities that may cause device reboots or loss of functionality.

    Product
    Infinity Delta Family patient monitors The Infinity Delta Series (Delta/Delta XL/Kappa) monitors are intended to be used on adult, pediatric, and neonatal populations, with the exception of the parameter Cardiac Output, ST Segment Analysis, and arrhythmia which are intended…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0970-2019·2019-03-13

    Pentax C2 CryoBalloon Controller Recalled for Overpressure Detection Failure

    Pentax of America Inc is recalling 45 C2 CryoBalloon Controllers because the device fails to detect balloon overpressure during specific nitrous oxide applications, posing a risk of patient injury.

    Product
    C2 CryoBalloon Controller, REF: FG-1017, with Controller Software v1.18.258 The C2 CryoBalloon Ablation System is intended to be used as a cryosurgical tool in the field of general surgery, specifically for endoscopic application and the ablation of dysplastic Barrett s…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0983-2019·2019-03-13

    Maquet Cardiovascular Recalls AXIUS Blower Mister Due to CO2 Flow Issues

    Maquet Cardiovascular is recalling AXIUS Blower Mister devices because a potential lack of carbon dioxide flow may cause procedural delays during off-pump coronary artery bypass surgery.

    Product
    AXIUS Blower Mister Product Code/REF Number: CB-1000 The Axius Blower Mister is intended to clear an anastomotic site for improved visibility
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0981-2019·2019-03-13

    BD MAX Enteric Bacterial Panel Recalled for False Negative Results

    Becton Dickinson is recalling 1,583 BD MAX Enteric Bacterial Panel kits due to false negative results for specific bacterial targets.

    Product
    BD MAX Enteric Bacterial Panel -For In Vitro Diagnostic Use with the BD MAX System Catalog Number: 442963 The BD MAX Enteric Bacterial Panel performed on the BD MAX System is an automated in vitro diagnostic test for the direct qualitative detection and differentiation of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0865-2019·2019-03-13

    Raindrop Near Vision Inlay Recalled Due to Increased Risk of Corneal Haze

    RVO 2.0, Inc. is recalling Raindrop Near Vision Inlays because a post-approval study found an increased risk of corneal haze following implantation.

    Product
    Raindrop Near Vision Inlay, REF: RD1-1, Sterile, Rx Only, Manufacturer ReVision Optics, Inc.
    Category
    Medical Device
    Distribution
    37 states
  • CriticalFDA (Devices)·Z-0805-2019·2019-03-06

    ICU Medical Recalls ChemoLock Vial Spike Due to Potential Burr Particulate

    ICU Medical is recalling one lot of ChemoLock Vial Spike devices due to a potential for containing burr particulate. The recall covers 2,050 units distributed in the US and internationally.

    Product
    icumedical ChemoLock Vial Spike, 20mm, REF CL-80S The ChemoLock Closed System Drug Transfer Device prevents the transfer of environmental contaminants, including bacterial and airborne contaminants into the system, and the escape of drug or vapor concentrations outside the…
    Category
    Medical Device
    Distribution
    7 states
  • SevereFDA (Devices)·Z-0906-2019·2019-03-06

    Philips Achieva 3.0T MRI System Recalled for Ceiling Speaker Hazard

    Philips is recalling 11,226 Achieva 3.0T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Achieva 3.0T TX-series, Model Number 781278. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0907-2019·2019-03-06

    Philips Achieva MRI System Recalled for Falling Ceiling Speaker Hazard

    Philips is recalling Achieva 1.5T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Achieva 1.5T Conversion, Model Number 781283. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0922-2019·2019-03-06

    Philips Ingenia Elition S MRI System Recalled for Falling Speaker Hazard

    Philips is recalling Ingenia Elition S MRI systems because ceiling speakers may fall due to magnetic attraction.

    Product
    Ingenia Elition S, Model Number 781357. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0878-2019·2019-03-06

    Philips MRI System Recall Due to Ceiling Speaker Magnetic Hazard

    Philips is recalling Intera 1.5T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Intera 1.5T Power/Pulsar, Model Number 781105. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0886-2019·2019-03-06

    Philips Intera 1.5T MRI Systems Recalled for Falling Speaker Hazard

    Philips is recalling 11,226 Intera 1.5T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Intera 1.5T R11, Model Number 781170. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0917-2019·2019-03-06

    Philips Panorama 1.0T MRI Systems Recalled for Falling Speaker Hazard

    Philips is recalling 11,226 Panorama 1.0T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Panorama 1.0T, Model Number 781350. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0924-2019·2019-03-06

    Philips MR-OR 1.5T MRI Systems Recalled for Falling Speaker Hazard

    Philips is recalling 11,226 MR-OR 1.5T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    MR-OR 1.5T, Model Number 781437. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0884-2019·2019-03-06

    Philips Achieva XR MRI Systems Recalled for Ceiling Speaker Hazard

    Philips is recalling 11,226 Achieva XR MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Achieva XR 1.5T/3.0T, Model Number 781153. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0888-2019·2019-03-06

    Philips MRI System Recall Due to Ceiling Speaker Magnetic Hazard

    Philips is recalling Intera Achieva 1.5T Nova MRI systems because ceiling speakers may be pulled by the magnetic field and fall.

    Product
    Intera Achieva 1.5T Nova, Model Number 781172. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0927-2019·2019-03-06

    Philips Achieva 3.0T MRI System Recalled for Ceiling Speaker Hazard

    Philips is recalling Achieva 3.0T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Achieva 3.0T for PET, Model Number 781477. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0923-2019·2019-03-06

    Philips Ingenia Elition X MRI Systems Recalled for Falling Speaker Hazard

    Philips is recalling Ingenia Elition X MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Ingenia Elition X, Model Number 781358. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide