ClearanceBrief
Recall Z-1622-2010 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

Endotec, Inc.

Endotec Prosthesis Shoulder, Titanium Alloy, Sterilized Modular Femoral Stem BP Shoulder Component: 12mm Modular Femoral Stem, Catalog: 02-21-0103, Lot 02-21-0103ANN374.

DateMay 20, 2010 (initiated Jun 5, 2009)
StatusTerminated
ReasonEndotec 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 results.
Root causeOther
ActionRecall Letters were sent to each distributor on 06/07/2009. Questions are directed to Endotec at (407) 822-0021.
Quantity3 Pieces
DistributionWorldwide distribution -- US in OH, TX, CA, FL, NJ, TN; and International Distribution: Korea, Australia, Switzerland, The Netherlands, Spain. Domestic: OH, TX, CA, FL, NJ, TN.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K904880BUECHEL-PAPPAS HUMERAL STEM COMPONENT
Endotec, Inc., Jan 28, 1991