ClearanceBrief
Recall Z-1820-2009 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

Smith & Nephew Inc

LEGION Pressfit Stem, Straight, 20 MM X 160 MM, REF 71424053, Sterile, Smith & Nephew, Memphis TX 38116. The device is used for Orthopedic Knee Implants.

DateAug 23, 2009 (initiated Jan 22, 2009)
StatusTerminated
ReasonProducts were mispackaged.
Root causeProcess control
ActionAll affected Smith & Nephew Sales Representatives were notified of the problem and the recall via email and overnight mail on January 22, 2009. All affected Smith & Nephew International Distributors were notified via email and telephone on January 22, 2009. They were instructed to immediately quarantine the product for return.
Quantity19 units
DistributionWorldwide Distribution -- US, Canada, Australia, Germany, GB, Italy, Switzerland, Spain, and France.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K043440SMITH & NEPHEW, INC. REVISION KNEE SYSTEM
Smith & Nephew, Inc., Feb 18, 2005