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NuVasive Recalls Orthopedics Implants Over Biocompatibility Concerns

The US FDA says the company has voluntarily issued a recall for Precice metal implants after reports of adverse events that could be related to the design of the product or biocompatibility issues.

• Source: NuVasive

The US Food and Drug Administration is warning health care providers about potential biocompatibility and design issues with NuVasive’s specialized orthopedics Precice devices, which are made from steel and titanium. The agency says adverse events including pain, and changes in the surrounding bone and soft tissue have been record by patients implanted with the Precice Stryde, the steel version of the product.

The devices are intended for use by patients 18 and older to lengthen or compress their limbs or transport segments...

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