Urgent Worldwide Recall Of Zimmer’s PEEK Ardis® Interbody Spacer Inserter

Zimmer Spine, Inc. is initiating a voluntary worldwide recall of all 315 units of the PEEK Ardis® Inserter because of reports of implant breakage when the implant is subjected to excessive lateral and/or off-axis forces from the inserter during surgery.



Zimmer Spine Issues Urgent Worldwide Medical Device Recall of the Inserter Instrument for the PEEK Ardis® Interbody Spacer (via PR Newswire)

MINNEAPOLIS, Dec. 20, 2012 /PRNewswire/ — 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.  The inserters are being recalled…


published: December 20, 2012 in: Recalls, Spine, Zimmer

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