The Recall Desk

Severity 3 of 5

High recalls

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

What “high” means here

Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

26401–26425 of 50460

  • HighFDA (Devices)·Z-0942-2019·2019-03-06

    Arrow AutoFuser Disposable Pain Control Pump Recalled for Potential Cracks

    Arrow International Inc. is recalling 8 units of the Arrow AutoFuser Disposable Pain Control Pump due to possible cracks on the fill port connector that may cause leaks.

    Product
    AF550x5ML/H 2ML 60LO 6" CATH, 4.5" IN, Product code MT5060XLSK5 CP, Arrow AutoFuser Disposable Pain Control Pump
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0939-2019·2019-03-06

    Merge Eye Station Retinal Imager Recalled for Electrical Safety Defects

    Merge Healthcare is recalling 1,252 WinStation Retinal Imagers because certain configurations may produce electrical output exceeding allowable medical device limits.

    Product
    The WinStation Retinal Imager, also known as Merge Eye Station. DCF-1024 & DCF-512 Digital Imaging System Product Usage: The WinStation Retinal Imager has the same intended use as other fundus cameras. It is specifically used to produce color or black and white images of the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0949-2019·2019-03-06

    Arrow AutoFuser Disposable Pain Control Pump Recalled for Potential Cracks

    Arrow International Inc. is recalling 9 units of the Arrow AutoFuser Disposable Pain Control Pump due to possible cracks on the fill port connector that may cause leaks.

    Product
    AF 550 x 5ML/HR CPNB, Product code MC0050XL CPNB, Arrow AutoFuser Disposable Pain Control Pump
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0872-2019·2019-03-06

    Philips Multiva MRI System Recalled for Ceiling Speaker Hazard

    Philips is recalling Multiva 1.5T MRI systems because ceiling speakers may fall due to magnetic attraction.

    Product
    Multiva 1.5T 16 R5 (ZBO), Model Number 781073. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0887-2019·2019-03-06

    Philips MRI System Recall for Falling Ceiling Speaker Hazard

    Philips is recalling Intera Achieva 1.5T Pulsar MRI systems because ceiling speakers may fall due to magnetic attraction.

    Product
    Intera Achieva 1.5T Pulsar, Model Number 781171. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0961-2019·2019-03-06

    Alcon Ophthalmic Microscope Recalled for Potential Optical Head Detachment

    Alcon is recalling LuxOr E71 and E71 Q-Vue ophthalmic microscopes because the optical head may detach from the stand due to missing thread adhesive.

    Product
    Alcon or Endure Ophthalmic Microscope Product Usage: Used for low magnification visualization during ophthalmic surgical procedures for cataract, retina and cornea.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0925-2019·2019-03-06

    Philips MR-OR 3.0T MRI Systems Recalled for Falling Speaker Hazard

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

    Product
    MR-OR 3.0T, Model Number 781438. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0899-2019·2019-03-06

    Philips Achieva XR MRI Systems Recalled for Falling Speaker Hazard

    Philips is recalling 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 781253. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0909-2019·2019-03-06

    Philips Achieva MRI Systems Recalled Due to Ceiling Speaker Hazard

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

    Product
    Achieva 1.5T, Model Number 781296. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·19V171000·2019-03-05

    2019 Western Star Trucks Recalled for Odometer Unit Labeling Error

    Daimler Trucks North America is recalling 2019 Western Star 4700 and 4900 trucks because the odometer displays miles but tracks kilometers, potentially causing driver confusion.

    Product
    WESTERN STAR — WESTERN STAR 4700, 4900
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V170000·2019-03-05

    Thomas Built Buses Minotour Recalled for Wheelchair Lift Safety Defect

    Daimler Trucks North America is recalling 2003-2019 Thomas Built Buses Minotour school buses because the wheelchair lift can operate without the parking brake engaged, posing an injury risk.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES MINOTOUR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V162000·2019-03-04

    Darley Recalls 2017-2019 Fire Trucks Due to Brake Light Wiring Defect

    W. S. Darley & Co. is recalling 2017-2019 WASP fire trucks because brake lights may illuminate without the pedal being pressed, potentially confusing other drivers.

    Product
    DARLEY — DARLEY FIRE APPARATUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V163000·2019-03-04

    LDV Command Center and Emergency Response Vehicles Recalled for Brake Light Defect

    LDV, Inc. is recalling 2017-2018 Command Center and Emergency Response vehicles because brake lights may illuminate without the pedal being pressed, potentially confusing other drivers.

    Product
    LDV, INC. — LDV, INC. COMMAND CENTER, EMERGENCY RESPONSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V165000·2019-03-04

    KZRV Recalls 2019 RVs Due to Cooktop Flame Inversion Risk

    KZRV is recalling 2019 Sportsmen, Escape, and Sonic Lite trailers because the cooktop flame may invert, increasing burn risk.

    Product
    KZRV — KZRV SPORTSMEN, ESCAPE, SONIC LITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V156000·2019-03-01

    Indian Recalls 2019 Scout Motorcycles Due to Brake Performance Issues

    Indian Motorcycle is recalling 2019 Scout, Scout Bobber, and Scout Sixty models because trapped air in the brake system may reduce performance and increase crash risk.

    Product
    INDIAN — INDIAN SCOUT SIXTY, SCOUT, SCOUT BOBBER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V155000·2019-03-01

    Maintainer Recalls 2017-2018 Rescue Vehicles Due to Brake Light Wiring Issue

    Maintainer is recalling 2017-2018 MCB Custom Bodies Responders/Rescue Walkaround vehicles because Whelen brake lights may illuminate without the brake pedal being pressed, potentially confusing other drivers.

    Product
    MAINTAINER — MAINTAINER RESCUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V160000·2019-03-01

    Supreme Classic American Trolley Recall for Wheelchair Lift Defect

    Supreme is recalling 2014-2016 Classic American Trolley vehicles because a wheelchair lift cam may fail, causing the platform to rise too high and increasing injury risk.

    Product
    SUPREME — SUPREME CLASSIC AMERICAN TROLLEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V159000·2019-03-01

    Marion Fire and Emergency Apparatus Brake Light Recall

    Marion is recalling 2017-2018 Fire and Emergency Apparatus vehicles because Whelen brake lights may illuminate without the brake pedal being pressed.

    Product
    MARION — MARION FIRE AND EMERGENCY
    Category
    Vehicle
    Distribution
    Distributed nationwide