FDAApril 15, 2016device
00720504022 ACETAB.CUPW/SH,0DEG,22MMX40MM 00720504222 ACETAB.CUPW/SH,0DEG,22MMX42MM 00720504622 ACETAB.CUPW/SH,0DEG,22MMX46MM 00720504828 ACETAB.CUPW/SH,0DEG,28MMX48MM 00720505228 ACETAB.CUPW/SH,0DEG,28MMX52MM 00720505628 ACETAB.CUPW/SH,0DEG,28MMX56MM 00720505828 ACETAB.CUPW/SH,0DEG,28MMX58MM 007...
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Zimmer Biomet is initiating a recall of specific lots of foil pouched, sterile Trabecular Metal implants that were manufactured between April 2011 and October 2012. The foil pouches are part of a dual barrier system to provide sterile integrity.
What to do
FDA enforcement status: Terminated
Brands named
zimmer trabecular metal technologyzimmerzimmer trabecular
UPCs
007205040220072050422200720504622007205048280072050522800720505628007205058280072050602800720506228007205064280072100422200721004422
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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