Stryker Accolade TMZF Hip Stem Lawsuit Filed Over Implant Failure
A lawsuit indicates that the combination of a Stryker Accolade TMZF hip stem with the recalled Stryker L-Fit V40 femoral head caused severe complications for a Minnesota man.…
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A lawsuit indicates that the combination of a Stryker Accolade TMZF hip stem with the recalled Stryker L-Fit V40 femoral head caused severe complications for a Minnesota man.…
A lawsuit filed by a New York woman says that components in a Stryker hip replacement system, including its LFit V40 and Accolade components, failed, resulting in loss of mobility, pain, and the need for revision surgery.…
Canada recalled the Stryker LFit V40 femoral head hip components days before the manufacturer sent a warning to doctors around the world that they were prone to failure.…
Problems with Stryker LFIT V40 Femoral Head components used during may hip replacement procedures have been linked to a higher-then-expected failure rate, according to a recent warning.…
Australian officials warn that some Stryker LFIT femoral head hip replacement system components appear to have high failure rates.…
A catheter recall for some Stryker catheters has been rated a Class I medical recall by the FDA, which warns that reports of tip separations means that the devices could cause serious injury or death.…
Researchers warn that patients who undergo revision surgery to remove failed Stryker Rejuvenate modular hip systems face a 13% rate of complications.…
With Stryker Rejuvenate hip replacements continuing to fail, the judge presiding over the litigation issued an order requiring plaintiffs to file notice with the Court within 45 days after undergoing revision surgery.…
Stryker Rejuvenate hip lawsuits continue to be filed as plaintiffs experience failures after a global settlement last year.…
OtisMed, a subsidiary of Stryker Corp. has agreed to pay $80 million in fines and penalties for illegally selling knee surgery cutting guides without the FDA’s approval.…