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In August, Advanced Bionics announced that 16% of implants worldwide are defective. The numbers found by the renowned Hannover Hearing Center are even higher – of the 349 patients studied 50% were determined to be…
class 1 recall issued for the zimmer biomet comprehensive reverse shoulder The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries…
FDA Recalls more than 40,000 Stryker LFIT Anatomic V40 Femoral Heads, Patients at Risk of Severe Injuries and Painful Replacement Surgeries In what may be one of the largest hip replacement device recalls in the…
stryker settlement announcement Latest settlement to pay restitution to numerous patients injured by Stryker Modular Rejuvenate and ABG II Femoral Hip Implants (Chicago – December 19, 2016) – The Multidistrict Litigation (MDL) Plaintiffs’ lead counsel…
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