ClearanceBrief
Recall Z-0909-2010 ยท LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented

Stryker Howmedica Osteonics Corp.

Trident Acetabular Hip System Polyethylene Inserts, Stryker Orthopaedics, multiple sizes, Mahwah, NJ. Intended for use in cementless fixation fro use in total hip arthroplasty to relieve pain and restore function in the hip.

DateMar 2, 2010 (initiated Feb 17, 2006)
StatusTerminated
ReasonStryker Orthopaedics became aware of a potential anomaly related to the packaging process of referenced lots of X# polyethylene used on Scorpio, Triathlon and Trident inserts.
Root causeProcess design
ActionStryker Orthopaedics issued an "Important Market Withdrawal" notification dated February 17, 2007 via federal express. Consignees were informed of the affected product and asked to retrieve, reconcile and return product via Return Material Authorization to the firm. For further information, contact Stryker Orthopaedics Quality Assurance at 1-201-831-5825.
Quantity594 units total - all products.
DistributionWorldwide Distribution -- United States and Canada.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K033716TRIDENT ACETABULAR SYSTEM
Howmedica Osteonics Corp., Feb 10, 2005