Zimmer Spine Issues Urgent Worldwide Medical Device Recall Of The Inserter Instrument For The PEEK Ardis Interbody Spacer

[Date Prev][Date Next][Thread Prev][Thread Next][Date Index][Thread Index]

 



Title: Zimmer Spine Issues Urgent Worldwide Medical Device Recall Of The Inserter Instrument For The PEEK Ardis Interbody Spacer

You are subscribed to Recalls, Market Withdrawals and Safety Alerts for U.S. Food & Drug Administration (FDA).

This information has recently been updated and is now available.

 

12/20/2012 01:58 PM EST

Zimmer Spine, Inc. is initiating a voluntary worldwide recall of all 315 units of the PEEK Ardis Inserter. The Ardis Inserter is a surgical instrument used during spinal surgery to implant the PEEK Ardis Interbody Spacer.

. For detailed information pertaining to this Recalls, Market Withdrawals and Safety Alerts message, please click the link at the beginning of this bulletin.


This email was sent to list-fda@xxxxxxxxxxx using GovDelivery, on behalf of: U.S. Food & Drug Administration (FDA) · 10903 New Hampshire Ave · Silver Spring, MD 20993 · 800-439-1420 Powered by GovDelivery

[Index of Archives]     [CDC News]     [NIH News]     [USDA News]     [Steve's Art]     [Camping in Yosemite]     [PhotoForum]     [SB Lupus]     [STB]

  Powered by Linux