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

20926–20950 of 40124

  • HighFDA (Devices)·Z-1200-2019·2019-04-24

    GE Healthcare Recalls Innova IGS 630 X-Ray Systems for Imaging Loss

    GE Healthcare is recalling 49 Innova IGS 630 Interventional Fluoroscopic X-Ray Systems due to a potential loss of x-ray imaging function when changing the field of view while releasing the footswitch.

    Product
    Innova IGS 630, Interventional Fluoroscopic X-Ray System used in generating fluoroscopic and rotational images of human anatomy for cardiovascular, vascular and non-vascular, diagnostic and interventional procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1183-2019·2019-04-24

    Gyrus ACMI Recalls Diego Elite Turbinate Blades Due to RF Activation Risk

    Gyrus ACMI is recalling 13 Diego Elite Turbinate Blades because they may allow unintended RF energy activation when used with compatible consoles.

    Product
    Diego Elite Turbinate Blades Bipolar Blade, 4mm curved, Product Number: BB4040SC
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1201-2019·2019-04-24

    GE Healthcare Recalls Innova IGS 6 X-Ray Systems Due to Imaging Loss

    GE Healthcare is recalling 22 Innova IGS 6 Interventional Fluoroscopic X-Ray Systems because they may lose x-ray imaging function during specific field of view changes.

    Product
    Innova IGS 6, Interventional Fluoroscopic X-Ray System used in generating fluoroscopic and rotational images of human anatomy for cardiovascular, vascular and non-vascular, diagnostic and interventional procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1139-2019·2019-04-24

    Pintler Medical Recalls 24 Warming Pads Due to Malfunction

    Pintler Medical LLC is recalling 24 warming pads used in operating rooms because they malfunction. The affected units were distributed to facilities in Wisconsin.

    Product
    A warming pad, a component of the PINTLER PEAK & PINTLER SUMMIT Heated OR pad. PPWS-001 indicated for use in any condition where patient warming is desired as determined by clinical personnel, in accordance with facility normo-thermia protocol
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-1132-2019·2019-04-24

    Wilson-Cook Recalls Acusnare Polypectomy Snares Due to Loop Retraction Issues

    Wilson-Cook Medical Inc. is recalling 34,456 Acusnare Polypectomy Snares because the snare loop may not completely retract or may misshape.

    Product
    Acusnare Polypectomy (Duck Bill Shaped) Snare Used with an electrosurgical unit for endoscopic polypectomy.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1178-2019·2019-04-24

    Olympus Diego Elite Console Recall for Unintended RF Energy Activation

    Gyrus ACMI is recalling Olympus Diego Elite Consoles because they may inadvertently activate the RF energy feature when used with specific blades.

    Product
    Olympus Diego Elite Console MDCONS 100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1196-2019·2019-04-24

    Abbott Alinity i Processing Module Recalled for Safety Interlock Defect

    Abbott is recalling Alinity i Processing Modules because a safety interlock may fail to deploy when a bulk solution bottle is removed.

    Product
    Abbott Alinity i Processing Module LN 03R65-01 - Product Usage: The Alinity i processing module is a fully automated immunoassay analyzer allowing random and continuous access, as well as priority and automated retest processing using chemiluminescent microparticle immunoassay…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1150-2019·2019-04-24

    Integra Salto Talaris Ankle Prosthesis Recalled for Incorrect Labeling

    Integra LifeSciences is recalling Salto Talaris and Integra XT Revision ankle implants because the labels list an incorrect metallic coating material symbol.

    Product
    Salto Talaris, Tibial Total Ankle Prosthesis Tray, Talar Dome, Size 0, Right, Part No. LJU200T
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Devices)·Z-1144-2019·2019-04-24

    Philips Brilliance iCT CT Scanners Recalled for Collimator Compensator Failure

    Philips is recalling two Brilliance iCT CT scanners because a component may fail, causing image artifacts. The devices were distributed only to China and the UK.

    Product
    Brilliance iCT, 728306 Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. This device may include signal analysis and display…
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1173-2019·2019-04-24

    Integra Talar Dome Total Ankle Prosthesis Recalled for Labeling Error

    Integra LifeSciences is recalling Talar Dome Total Ankle Prostheses because the labels and instructions for use list an incorrect metallic coating material symbol.

    Product
    Talar Dome Total Ankle Prosthesis , Sloped, Size 1, Left, Product No. LJV191T
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Devices)·Z-1138-2019·2019-04-24

    Topcon IMAGEnet 6 Software Recalled for Patient Data Display Error

    Topcon Medical Systems is recalling IMAGEnet 6 software due to a defect that may display incorrect patient identification information alongside thumbnails.

    Product
    IMAGEnet 6 v1.53- IMAGEnet 6 Ophthalmic Data System is a software program that is intended for use in the collection, storage and management of digital images, patient data, diagnostic data and clinical information from Topcon devices without controlling or altering the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1166-2019·2019-04-24

    Integra Talar Dome Total Ankle Prosthesis Recalled for Labeling Error

    Integra LifeSciences is recalling Talar Dome Total Ankle Prostheses because the labels and instructions for use list an incorrect metallic coating material symbol.

    Product
    Talar Dome Total Ankle Prosthesis , Flat Cut, Size 2, Right, Product No. LJU812T
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Devices)·Z-1175-2019·2019-04-24

    Integra Talar Dome Ankle Prosthesis Recalled for Incorrect Labeling

    Integra LifeSciences is recalling Talar Dome Total Ankle Prostheses because the labels and instructions for use list an incorrect metallic coating material symbol.

    Product
    Talar Dome Total Ankle Prosthesis , Sloped, Size 3, Left, Product No. LJV193T
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Devices)·Z-1168-2019·2019-04-24

    Integra Talar Dome Ankle Prosthesis Recalled for Incorrect Labeling

    Integra LifeSciences is recalling Talar Dome Total Ankle Prostheses because the labels incorrectly identify the metallic coating material.

    Product
    Talar Dome Total Ankle Prosthesis , Sloped, Size 0, Right, Product No. LJV180T
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Devices)·Z-1174-2019·2019-04-24

    Integra Talar Dome Ankle Prosthesis Recalled for Labeling Error

    Integra LifeSciences is recalling Talar Dome Total Ankle Prostheses because the labels incorrectly list the metallic coating material symbol.

    Product
    Talar Dome Total Ankle Prosthesis, Sloped, Size 2, Left, Product No. LJV192T
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Devices)·Z-1171-2019·2019-04-24

    Integra Talar Dome Ankle Prosthesis Recalled for Incorrect Labeling

    Integra LifeSciences is recalling Talar Dome Total Ankle Prostheses because the labels incorrectly identify the metallic coating material.

    Product
    Talar Dome Total Ankle Prosthesis , Sloped, Size 3, Right, Product No. LJV183T
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Devices)·Z-1169-2019·2019-04-24

    Integra LifeSciences Recalls Talar Dome Ankle Prostheses Due to Labeling Error

    Integra LifeSciences is recalling Talar Dome Total Ankle Prostheses because the labels and instructions for use list an incorrect metallic coating material symbol.

    Product
    Talar Dome Total Ankle Prosthesis , Sloped, Size 1, Right, Product No. LJV181T
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Devices)·Z-1141-2019·2019-04-24

    Philips Medical Systems Recalls Foot Switches for Allura Xper Systems

    Philips Medical Systems is recalling 7,209 foot switches used with Allura Xper systems because pedals may bend, causing an inability to make live fluoroscopy images or exposures.

    Product
    Foot Switches used with the following systems: 722001 Allura Xper FD 10 C 722002 Allura Xper FD10 F 722003 Allura Xper FD10 722005 Allura Xper FD10/10 722006 Allura Xper FD20 722008 Allura Xper FD20 Biplane 722010 Allura Xper FD10 722011 Allura Xper FD10/10 722012…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1135-2019·2019-04-24

    Ethicon Recalls VICRYL Plus Sutures Due to Labeling Mismatches

    Ethicon, Inc. is recalling VICRYL Plus Sutures because the product may not match the sales unit carton and foil label.

    Product
    VICRYL PLUS Sutures: VICRYL PLUS SUTURE 18"(45CM) 3-0 VIO VICRYL PLUS SUTURE 18"(45CM) 0 UND VICRYL PLUS SUTURE 18"(45CM) 0 VIO VICRYL PLUS SUTURE 18"(45CM) 0 VIO) VICRYL PLUS SUTURE 18"(45CM) 1 VIO VICRYL PLUS SUTURE 18"(45CM) 4-0 VIO VICRYL PLUS SUTURE 27"(70CM) 3-0…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1154-2019·2019-04-24

    Salto Talaris Ankle Prosthesis Recalled for Incorrect Labeling

    Integra LifeSciences is recalling Salto Talaris Tibial Total Ankle Prosthesis trays due to incorrect metallic coating material symbols on labels and instructions.

    Product
    Salto Talaris Tibial Total Ankle Prosthesis Tray, Talar Dome, Size 0, Left, Part No. LJU210T
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Devices)·Z-1160-2019·2019-04-24

    Integra Tibial Total Ankle Prosthesis Tray Recalled for Labeling Errors

    Integra LifeSciences is recalling Tibial Total Ankle Prosthesis Trays due to incorrect metallic coating symbols on labels and instructions.

    Product
    Tibial Total Ankle Prosthesis Tray, Size 2, Product No. LJU222T
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Devices)·Z-1143-2019·2019-04-24

    Philips Brilliance 64 CT Systems Recalled for Image Artifacts

    Philips is recalling 14 Brilliance 64 CT systems because a component may fail, causing ring or smudge artifacts on images.

    Product
    Brilliance 64, 728231 Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. This device may include signal analysis and display…
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1158-2019·2019-04-24

    Integra Tibial Total Ankle Prosthesis Tray Recalled for Labeling Error

    Integra LifeSciences Corp. is recalling Tibial Total Ankle Prosthesis Trays because the labels list an incorrect metallic coating material symbol.

    Product
    Tibial Total Ankle Prosthesis Tray, Size 0, Product No. LJU220T
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Devices)·Z-1152-2019·2019-04-24

    Integra Recalls Salto Talaris Ankle Prosthesis Due to Labeling Error

    Integra LifeSciences is recalling Salto Talaris Tibial Total Ankle Prosthesis trays because the labels list an incorrect metallic coating material symbol.

    Product
    Salto Talaris Tibial Total Ankle Prosthesis Tray, Talar Dome, Size 2, Right, Part No. LJU202T
    Category
    Medical Device
    Distribution
    26 states