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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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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, which can...

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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 failed? Do...

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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 company may...

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Australian 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 of femoral...

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New Stryker Hip Recall Update and Top 5 Things Patients Need To Know

  The FDA in April of 2016 updated its website regarding recommendations about soft tissue imaging and metal ion testing....

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Broadspire Reimbursement Process-Guidelines on Hip Implant Recalls

At Childers, Schlueter & Smith we have handled hundreds of hip implant replacement claims for clients all over the country...

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Broadspire Reimbursement Process For Recalled DePuy ASR or Stryker Rejuvenate or ABGII Claims.

We encourage hip implant patients with recalled devices to consult a lawyer before talking with Broadspire, but if you choose to...

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Pinnacle Hip Lawsuits Move Forward

According to an April Order, the U.S. District Court, Northern District of Texas has amended an earlier Case Management Order...

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Complications Linked to DePuy Pinnacle Hip Replacement System

If 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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