Thursday 2nd February 2012
by admin
A hip system may possibly be recalled by the manufacturer for a quantity of reasons. If your device is recalled, this does not necessarily mean that the device wants to be removed and replaced. In some circumstances the recall just calls for different or a lot more frequent monitoring. It is crucial to talk about the cause for the recall with your surgeon to figure out the most appropriate course of action. If you or someone you know have had a Depuy Hip implant learn more about the products that have been recalled.
DePuy ASR&trade XL Acetabular Strategy
On August 24, 2010, there was a voluntary recall of the DePuy ASR&trade total hip plan because of new, unpublished details from the UK joint registry indicating the revision rates inside 5 years had been around 13 percent.
Zimmer Durom® Acetabular Component
On July 22, 2008, there was a voluntary recall of the Zimmer Durom® Acetabular Component (“Durom Cup”) basically due to the fact the directions for use/surgical approach directions were inadequate. People who have had one of these and other Depuy hip replacements may be interested in pursuing Depuy Hip litigation against the manufacturer.