A hip implant may be recalled by the manufacturer for a number of reasons. If your hip implant is recalled, this does not necessarily mean that the implant needs to be removed and replaced. In some cases the recall recommends different or more frequent monitoring. It is important to discuss the reason for the recall with your orthopedic surgeon to determine the most appropriate course of action.
Smith & Nephew R3 Metal Liners of the R3 Acetabular System
On June 1, 2012 Smith & Nephew Orthopedics initiated a market withdrawal for metal liners of the R3 acetabular system due to a higher than expected number of revision surgeries associated with the use of the device in total hip replacements outside the US.
Smith & Nephew is recommending that physicians maintain their usual follow-up protocol for patients who have undergone total hip replacement or resurfacing surgery.
In the US:
DePuy ASRÔ XL Acetabular System
- The R3 metal liner is only approved for use with the Birmingham Hip Resurfacing System.
- The R3 Acetabular System is a total hip replacement system component that is not cleared for use with the R3 metal liner.
On Aug. 24, 2010, there was a voluntary recall of the DePuy ASR TM total hip system because of new, unpublished data from the UK joint registry indicating the revision rates within 5 years were approximately 13 percent.
Note: UK joint registry data is indicative of revision rates only in the UK and may not necessarily directly correlate to revision rates in the US.
For additional information about this recall, as provided by DePuy, see ASRÔ Hip System Recall Guide
. The preceding link is to a website owned and operated by DePuy Companies.
Zimmer Durom® Acetabular Component
On July 22, 2008, there was a voluntary recall of the Zimmer Durom® Acetabular Component ("Durom Cup") because the instructions for use/surgical technique instructions were inadequate. Class 2 Device Recall Durom cup
Helping Defective Hip Replacement Recipients In Wisconsin