The Zimmer Durom Cup is the component most often cited in
Zimmer hip litigation, and it is theorized that as many as 12,000 plaintiffs
could join the ever-growing Zimmer litigation. Settlements will depend on the
amount of suffering and the nature of the side effect a plaintiff has had to
endure as well as the number of patients involved.The Zimmer Durom Cup
hip implant was first introduced in the United States in 2006, with a design
that was supposed to avoid many problems associated with traditional hip
replacement components. However, shortly after it was introduced, concerns
emerged about a high number of Zimmer
hip replacement recall failures involving the Durom Cup, where the component loosened
and required Zimmer hip revision surgery.
No Zimmer hip settlements are expected until late 2011 or 2012 as the Zimmer hip MDL
proceeds. While Zimmer’s own estimates in 2008 suggested that some doctors
experienced failure rates as high as 5.7%, some claims have suggested that the
between 20% and 30% of people may experience Zimmer Durom Cup hip
problems.
Zimmer intends to reintroduce the artificial hip implant after they develop instructions about the special surgical techniques that doctors need to use to avoid the risk of Durom Cup problems. Many of the problems associated with Zimmer hip failure surface over time and it is expected that, as these problems come to light, the number of Zimmer hip lawsuits will swell into one of the largest MDL as of yet.
Zimmer intends to reintroduce the artificial hip implant after they develop instructions about the special surgical techniques that doctors need to use to avoid the risk of Durom Cup problems. Many of the problems associated with Zimmer hip failure surface over time and it is expected that, as these problems come to light, the number of Zimmer hip lawsuits will swell into one of the largest MDL as of yet.
A Zimmer Durom Cup recall was not issued, since they indicated that there was no manufacturing
defect or design defect with the components. They indicated that sales would be
resumed once additional product labeling was developed to provide instructions
about special surgical techniques that are required to avoid problems. They
also indicated that a new surgical training program would be implemented in the
United States, since the technology and design parameters of the Durom Cup
require a higher degree of precision than the more common hip replacement
surgical techniques used in the United States. Surgeons have refuted that claim
and, instead, argue that the blame lay on faulty design plans carried out by
Zimmer Inc.
No comments:
Post a Comment