ClearanceBrief
Recall Z-1933-2008 ยท MEH Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate

Portland Orthopaedics Pty, Ltd.

Margron DTC Hip Replacement System; Margron hip - Femoral neck AZ, sterile, Portland Orthopaedics Inc., St. Clair, MI; REF 1-750-000. Product is used for Orthopedic surgery.

DateSep 18, 2008 (initiated Jan 11, 2008)
StatusTerminated
ReasonAustralian data indicates the product is associated with a higher than average rate of hip replacement revision surgery.
Root causeDevice Design
ActionStocks were pulled from U.S. consignees on or before 1/11/08. Consignee and implanting surgeon letters dated 6/20/08 were sent advising of the issue and recommending patient monitoring. For assistance, contact Portland Orthopaedics at 1-810-329-3348.
Quantity2403 of all products
DistributionNationwide.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K032641MODIFICATION TO: THE MARGRON HIP REPLACEMENT SYSTEM
Portland Orthopaedics Pty. , Ltd., Jan 20, 2004
K992815THE MARGRON HIP REPLACEMENT SYSTEM
Portland Orthopaedics Pty. , Ltd., Feb 7, 2000