Recall of Device Recall Ingenuity TF PET/CT

According to U.S. Food and Drug Administration, this recall involved a device in United States that was produced by Philips Medical Systems (Cleveland) Inc.

What is this?

A correction or removal action taken by a manufacturer to address a problem with a medical device. Recalls occur when a medical device is defective, when it could be a risk to health, or when it is both defective and a risk to health.

Learn more about the data here
  • Type of Event
    Recall
  • Event ID
    64403
  • Event Risk Class
    Class 2
  • Event Number
    Z-0897-2013
  • Event Initiated Date
    2013-01-21
  • Event Date Posted
    2013-02-28
  • Event Status
    Terminated
  • Event Country
  • Event Terminated Date
    2013-07-19
  • Event Source
    USFDA
  • Event Source URL
  • Notes / Alerts
    U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
    The Parent Company was added by ICIJ.
    The parent company information is based on 2017 public records.
  • Extra notes in the data
    System, tomography, computed, emission - Product Code KPS
  • Reason
    The system may not default to the same gating trigger with which the data were acquired. this could cause a risk for patients.
  • Action
    Philips Medical Systems (Cleveland), Inc. sent an "URGENT-MEDICAL DEVICE CORRECTION" letter dated January 21, 2013 to the affected customer. The letter identified the product, problem, and actions to be taken by the customer. Contact your local Philips representative or Philips Healthcare office for further information concerning this issue.

Device

  • Model / Serial
    Model # 882456, Serial # 2004. Units currently running Ingenuity TF PET/CT system software version 4.0.0.26635.
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Distributed only in Ohio.
  • Product Description
    Ingenuity TF PET/CT. Diagnostic imaging system
  • Manufacturer

Manufacturer

  • Manufacturer Address
    Philips Medical Systems (Cleveland) Inc, 595 Miner Rd, Cleveland OH 44143-2131
  • Manufacturer Parent Company (2017)
  • Source
    USFDA