ClearanceBrief
Recall Z-1950-2016 ยท MBH Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer

Zimmer Trabecular Metal Technology, Inc.

POROUS PATELLA 32MM X 10MM - 00587806532 POROUS PATELLA 35MM X 10MM- 00587806535 POROUS PATELLA 38MM X 10MM - 00587806538 POROUS PATELLA 41MM X 10MM - 00587806541

DateApr 15, 2016
StatusTerminated
ReasonZimmer 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.
Root causeUnknown/Undetermined by firm
ActionZimmer issued an Urgent Medical Device Recall Letter dated 4/15/2016.
Quantity19,884 total
DistributionNationwide and Foreign.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K031462THE NEXGEN KNEE SYSTEM UNCEMENTED COMPONENTS
Implex Corp., Aug 6, 2003