FDA Warns of Risk Related to Stryker’s STAR Ankle Replacement
The U.S. Food and Drug Administration (FDA) issued a warning on March 15, 2021, advising patients and medical providers regarding...
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The U.S. Food and Drug Administration (FDA) issued a warning on March 15, 2021, advising patients and medical providers regarding...
Learn MoreThe Stryker LFIT Anatomic Cobalt Chromium (CoCr) V40 femoral head had a limited voluntary recall in August, 2016, which can...
Learn MoreDo you have a defective knee that needs to be replaced or revised? Do you know why it failed? Do...
Learn MoreStryker has faced numerous hip replacement recalls and lawsuits in the past, and it seems likely that the company may...
Learn MoreAustralia’s Therapeutic Goods Administration, in consultation with Stryker Orthopaedics, recently issued a hazard alert for a specific range of femoral...
Learn MoreThe FDA in April of 2016 updated its website regarding recommendations about soft tissue imaging and metal ion testing....
Learn MoreAt Childers, Schlueter & Smith we have handled hundreds of hip implant replacement claims for clients all over the country...
Learn MoreWe encourage hip implant patients with recalled devices to consult a lawyer before talking with Broadspire, but if you choose to...
Learn MoreAccording to an April Order, the U.S. District Court, Northern District of Texas has amended an earlier Case Management Order...
Learn MoreIf you have experienced problems or complications after receiving a hip replacement utilizing the DePuy Pinnacle metal-on-metal hip implant system,...
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