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
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Limited Voluntary Recall of Stryker LFIT Anatomic Cobalt Chromium V40 Femoral Head
The Stryker LFIT Anatomic Cobalt Chromium (CoCr) V40 femoral head had a limited voluntary recall in August, 2016,
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Knee Replacement Revision Surgery: Did the manufacturer fail you?
Do you have a defective knee that needs to be replaced or revised? Do you know why it
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Stryker Hip Replacement Problems Continue
Stryker has faced numerous hip replacement recalls and lawsuits in the past, and it seems likely that the
Learn MoreAustralian Government Issues New Alert Regarding Stryker Hip Implant LFIT V40 Metal Heads
Australia’s Therapeutic Goods Administration, in consultation with Stryker Orthopaedics, recently issued a hazard alert for a specific range
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