Recall of Zimmer Alumina ceramic femoral head; 26 mm diameter alumina head with a +3.5 neck length on Co-Cr tapers. Cat. No. 6418-28-03

According to U.S. Food and Drug Administration, this recall involved a device in United States that was produced by Zimmer 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
    25257
  • Event Risk Class
    Class 2
  • Event Number
    Z-0461-03
  • Event Initiated Date
    2003-01-06
  • Event Date Posted
    2003-01-23
  • Event Status
    Terminated
  • Event Country
  • Event Terminated Date
    2003-12-04
  • 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
    Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented - Product Code LZO
  • Reason
    Compression test results are not in accordance with device approval submission.
  • Action
    Products distributed to the U.S. market are being recalled via letter to users dated 1/6/2003, which was sent via certified mail. Customers are being asked to return product on hand to Zimmer.

Device

  • Model / Serial
    all lots.
  • Product Classification
  • Device Class
    2
  • Implanted device?
    Yes
  • Distribution
    United States.
  • Product Description
    Zimmer Alumina ceramic femoral head; 26 mm diameter alumina head with a +3.5 neck length on Co-Cr tapers. Cat. No. 6418-28-03
  • Manufacturer

Manufacturer

  • Manufacturer Address
    Zimmer Inc., 345 E. Main St., Warsaw IN 46580
  • Source
    USFDA