ClearanceBrief
Recall Z-0476-2007 ยท KWL Prosthesis, Hip, Hemi-, Femoral, Metal

Stryker Howmedica Osteonics Corp.

Howmedica Hip Fracture Stem System No. 4 Femoral Component Fenestrated Sterile REF Catalogue #6942-0-040 Made in Ireland

DateJan 13, 2007 (initiated Nov 28, 2006)
StatusTerminated
ReasonLack of assurance of Sterility (package integrity): Anomalies in seal width and strength that may affect the integrity of the sterile barrier.
Root causeOther
ActionRecall notification letters and product accountability forms were sent on 11/29 via Fed Ex with return receipt.
Quantity67 units
DistributionNationwide
FDA recordOpen on fda.gov

510(k) clearances named in this recall

This recall record lists no 510(k) number.