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

Agency

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

Category

All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

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

Clear filters

27876–27900 of 40233

  • ModerateFDA (Devices)·Z-0949-2017·2017-01-11

    Merit PreludeEASE Hydrophilic Sheath Introducer Dilator Recall

    Merit Medical Systems is recalling 335 PreludeEASE Hydrophilic Sheath Introducer Dilators because the tips are undersized and cannot pass a 0.021-inch guide wire.

    Product
    PreludeEASE Hydrophilic Sheath Introducer Dilator The Merit PreludeEASE Hydrophilic Sheath Introducer is intended to provide access and facilitate the percutaneous introduction of various devices into veins and/or arteries, including but not limited to the radial artery, while…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0943-2017·2017-01-11

    MicroPort Orthopedics Recalls Profemur R Rasp Handles Due to Machining Issues

    MicroPort Orthopedics is recalling 20 units of Profemur R Rasp Handles because machining issues may prevent them from properly mating with broaches.

    Product
    PROFEMUR(R) R RASP HANDLE, REF PPW38078, 1 EACH, NON-STERILE, MicroPort Orthopedics, Arlington, TN Instruments support the implantation of implants. Broach handles mate to the broach to allow for preparation of the femoral canal for the stem component to be implanted. This
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0940-2017·2017-01-11

    Infraredx Recalls TVC Imaging System Due to Image Appearance Issues

    Infraredx, Inc. is recalling seven TVC Imaging System units because near-infrared images sometimes displayed lipid core plaques with an unusual horizontal orientation.

    Product
    TVC Imaging System model TVC-MC9 , for the near-infrared examination of coronary arteries in patients undergoing invasive coronary angiography The TVC Imaging System is an intravascular imaging device that simultaneously assesses vessel composition and structure using…
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-0919-2017·2017-01-04

    Siemens Recalls SOMATOM Scope CT Systems for Power Cutout Risk

    Siemens is recalling 13 SOMATOM Scope CT systems to replace a component that could cause a power cutout during use.

    Product
    SOMATOM Scope, Computed tomography x-ray system
    Category
    Medical Device
    Distribution
    10 states
  • HighFDA (Devices)·Z-0928-2017·2017-01-04

    Allen Medical Systems Recalls Arthex S3 Arm Sleeve Connectors

    Allen Medical Systems is recalling 420 Arthex S3 Arm Sleeve Connectors because they may separate unexpectedly during use, potentially causing moderate injury to patients.

    Product
    Arthex S3 Arm Sleeve Connector; Catalog Number AR-1650-02; manufactured and distributed between March and November 2016.
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-0916-2017·2017-01-04

    GE Healthcare Recalls X-Ray Systems Due to CRT Monitor Fall Risk

    GE Healthcare is recalling specific X-ray systems because aged CRT monitors may fall. The recall covers 1,598 units distributed in the US and internationally.

    Product
    SFX
    Category
    Medical Device
    Distribution
    41 states
  • HighFDA (Devices)·Z-0906-2017·2017-01-04

    GE Healthcare Recalls CRT Monitors Due to Potential Fall Hazard

    GE Healthcare is recalling specific CRT monitors due to the potential for the units to fall. The recall affects multiple system models including ADVANTX and Prestige.

    Product
    ADVANTX LCLP+
    Category
    Medical Device
    Distribution
    41 states
  • HighFDA (Devices)·Z-0901-2017·2017-01-04

    Medtronic NIM EMG Endotracheal Tubes Recalled for Exposed Wire Hazard

    Medtronic Xomed is recalling NIM EMG Endotracheal Tubes because wire in the tubing can become exposed, posing potential harm to intubated patients.

    Product
    NIM EMG Endotracheal Tube, 6.0 mm I.D. x 8.8 mm O.D. (27 FR), Reinforced, Sterile, Rx only. Individually packaged.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0918-2017·2017-01-04

    Shimadzu X-ray High Voltage Generator Recalled for Oil Leak Risk

    Shimadzu Medical Systems is recalling 13 X-ray high voltage generators due to a potential oil leak from the x-ray tube housing.

    Product
    Shimadzu X-ray High Voltage Generator Model No. UD150B-40 on SONIALVISION safire II/17 systems with 0.7/1.2JG326D X-Ray Tube Diagnostic x-ray high voltage generator.
    Category
    Medical Device
    Distribution
    7 states
  • HighFDA (Devices)·Z-0921-2017·2017-01-04

    Siemens Recalls CT Systems for Potential Power Cutout Defect

    Siemens is recalling 13 SOMATOM Perspective CT systems to replace a component that could cause power cutouts during use.

    Product
    SOMATOM Perspective, Computed tomography x-ray system
    Category
    Medical Device
    Distribution
    10 states
  • HighFDA (Devices)·Z-0909-2017·2017-01-04

    GE Healthcare Recalls Legacy Systems Due to CRT Monitor Fall Risk

    GE Healthcare is recalling Legacy and other imaging systems because aged CRT monitors may fall. The recall covers 1,598 units distributed in the US and internationally.

    Product
    Legacy
    Category
    Medical Device
    Distribution
    41 states
  • ModerateFDA (Devices)·Z-0902-2017·2017-01-04

    PerkinElmer Recalls Specimen Gate Laboratory Software Due to Disk Space Issue

    PerkinElmer Health Sciences is recalling 21 units of Specimen Gate Laboratory and eReports software because a defect may cause excessive disk space consumption, leading to software failure.

    Product
    Specimen Gate Laboratory 5002-0180, Specimen Gate eReports 5002-0370, Software Version 1.0 Specimen Gate Laboratory is intended for use as a data processing software used in the storage, retrieving, and processing of laboratory data. Specimen Gate eReports Software is a module…
    Category
    Medical Device
    Distribution
    12 states
  • ModerateFDA (Devices)·Z-0930-2017·2017-01-04

    Sterling Diagnostics Recalls HDL Cholesterol Kits Due to Expiration Date Error

    Sterling Diagnostics is recalling HDL Cholesterol diagnostic kits because previously extended expiration dates were rescinded.

    Product
    Sterling Diagnostics, Inc., HDL Cholesterol (PEF Method) for IN VITRO DIAGNOSTIC USE in the quantitative determination of analytes. These are CONSUMABLES - a customer buys another when kit is consumed.
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0875-2017·2017-01-04

    Neusoft NeuViz 64 CT Scanner Recall Due to Scan Interruption Error

    Neusoft Medical Systems is recalling 23 NeuViz 64 CT scanners because a software error may interrupt scans, requiring a system restart to resume.

    Product
    NeuViz 64 Multi-slice CT Scanner Systems
    Category
    Medical Device
    Distribution
    0 states