(b)(4).Initial reporter occupation: lawyer.If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.Investigation summary: no device associated with this report was received for examination.This hip replacement platform was voluntarily recalled from the market and the product codes are now considered inactive.Depuy considers the investigation closed.Should additional information be received, the information will be reviewed and the investigation will be re-opened as necessary.
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Asr revision.Litigation records received.Plaintiff alleges injury, economic loss, loss of services, loss of consortium, pain, excessive cobalt and chromium level and emotional distress.Doi: (b)(6) 2007, dor: (b)(6) 2018, left hip.
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