Why was DePuy forced to do a recall on their ASRhip implant products?

Studies indicate that as many as 1 in 8 patients with a DePuy ASR device have a hip implant that has been deemed defective by the manufacturer. DePuy has also learned that these patients have required an additional surgery to replace the device, also known as a "revision surgery."

by Jim Keller [email protected]

Partner at Keller & Keller

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Why was DePuy forced to do a recall on their ASRhip implant products?

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