More
than 150,000 Zimmer NexGen CR and Zimmer NexGen CR-Flex Porous Femoral implants
have been sold since 2003, and some doctors have reported experiencing a
substantially higher-than-expected rate of Zimmer knee failures within a few
years of surgery using these implants. This
Zimmer NexGen knee has a “high-flex” porous femoral component that attaches to
the bottom of the thighbone instead of using cement to keep the knee
replacements in place. The high-flexion (hi-flex) knee
implants, which promise a higher range of
motion than traditional devices, and are generally used in younger, more active
patients, but this appears to mean these patients more often require Zimmer knee revision surgery. Hi-flex knee replacement surgery requires that more bone at the back
of the knee be removed so
that the patient may bend the joint further farther.
However, the high-flexion coveted by many patients will not be achieved in
those whose mobility was very severely restricted before the surgery.
Zimmer
NexGen recalls have been issued for several different parts that may be used in
the company's complete knee replacement systems, including some Zimmer NexGen MIS and Zimmer NexGen LPS components. In
addition, research has linked a high rate of problems to some Zimmer NexGen CR-Flex knee replacement
components themselves. Following reports of at least 114 Zimmer NexGen knee replacement problems, the manufacturer issued a recall for Zimmer NexGen MIS
Tibial Components, NextGen TM Tibial Trays, NexGen MIS Modular Tibial Plates
and Keels. The Zimmer NexGen MIS knee recall affected more than 68,000 knee
components that were distributed throughout the United States.
According
to an order issued last month by the U.S. Judicial Panel on Multidistrict
Litigation, any individuals who file a Zimmer NexGen knee replacement lawsuit in federal district court will have their case consolidated as
part of an MDL, or multidistrict litigation. Although the cases will be managed
similar to how a Zimmer NexGen class action lawsuit would be handled
during pretrial proceedings, each claim will continue to remain an individual
lawsuit. It is expected that hundreds of lawsuits will eventually be filed
over Zimmer NexGen knee replacement problems, which involve early failure
of the artificial knee and often result in the need for additional revision
surgery.
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ReplyDeleteThe Knee replacement recall was due to software that caused a wider cutting range than needed. This meant patients suffered injuries and unstable joints, chronic pain, and limited movement.
ReplyDeleteThanks for the information, Keep up the good work!
Good Luck