LIFEPAK 1000 Defibrillators May Shut Down During Use, FDA Warns
Problems with the LIFEPAK 1000 defibrillator could cause a failure to deliver life-saving shocks, resulting in an FDA Class I recall classification.…
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Problems with the LIFEPAK 1000 defibrillator could cause a failure to deliver life-saving shocks, resulting in an FDA Class I recall classification.…
An Alabama man indicates that he experienced severe problems after a Stryker Accolade and Lfit V40 hip replacement fretted and corroded, resulting in the need for risky revision surgery to remove the components.…
Problems with the Stryker Accolade hip stem and Stryker LFit v40 femoral head caused a Massachusetts woman to experience complications associated with metal blood poisoning, which resulted in the need for revision surgery a few years after the artificial hip was implanted.…
Younger patients undergoing joint replacement surgery are more likely to need revision surgery to replace those implants later in life.…
As a growing number of hip replacement lawsuits continue to be filed by individuals who experienced problems from certain recalled Stryker femoral heads, requests have been filed to establish centralized pretrial proceedings in New Jersey state courts, as well as the federal court system.…
Although a growing number of Stryker hip lawsuits are being filed on behalf of individuals implanted with a recalled LFit v40 femoral head, the manufacturer is opposing centralization of the cases as part of a federal MDL.…
A motion to consolidate all Stryker LFit V40 femoral head lawsuits before one judge for pretrial proceedings has been filed with the U.S. JPML.…
A hip replacement lawsuit alleges that problems with a Stryker Accolade TMZF stem implanted with a Stryker LFit v40 femoral head caused high levels of cobalt to leach into a man’s body, resulting in premature failure of the artificial hip. …
A Stryker Rejuvenate and ABG II hip stem failure settlement agreement has been expanded to include patients who had to undergo revision surgery since the original 2014 settlement was reached.…
A product liability lawsuit filed against OtisMed, a subsidiary of Stryker, indicates that the company illegally sold cutting guides for knee replacement surgery that resulted in a woman’s knee implant failing, requiring revision surgery.…