Class 2 Device Recall Endotec, Prosthesis Knee - Food and Drug
https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=83196
WEBJun 5, 2009 · Endotec is recalling B-P Hip, B-P Shoulder, and B-P Knee Replacement System devices due to sterility issues involving validation, process variations and test … Date Initiated by Firm: June 05, 2009 Recall Number: Z-1621-2010 Date Posted: May 20, 2010 Recall Status 1: Terminated 3 on October 22, 2013
Date Initiated by Firm: June 05, 2009
Recall Number: Z-1621-2010
Date Posted: May 20, 2010
Recall Status 1: Terminated 3 on October 22, 2013
DA: 67 PA: 76 MOZ Rank: 55