Recall of Spine Clamp

According to U.S. Food and Drug Administration, this recall involved a device in United States that was produced by GE OEC Medical Systems,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
    30035
  • Event Risk Class
    Class 2
  • Event Number
    Z-0155-05
  • Event Initiated Date
    2004-09-15
  • Event Date Posted
    2004-11-03
  • Event Status
    Terminated
  • Event Country
  • Event Terminated Date
    2011-07-07
  • 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, Image Processing, Radiological - Product Code LLZ
  • Reason
    Threads on this accessory spine clamp may become tight, which may make it difficult to install or remove.
  • Action
    Consignees were notified by letter on 9/15/2004.

Device

  • Model / Serial
    Part Number: GE 1005556.
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    AL, CO, CA, FL, GA, LA, IL, IN, MA, MD, MI, MS, NC, NJ, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WI, WV, including one VA facility in TN. No military or foreign distribution.
  • Product Description
    Spine Clamp, an accessory to the InstaTrak 3500 Plus system. Clamp is attached to the spine to provide a mounting point for a transmitter.
  • Manufacturer

Manufacturer

  • Manufacturer Address
    GE OEC Medical Systems,Inc, 384 Wright Brothers Dr, Salt Lake City UT 84116-2862
  • Source
    USFDA