This follow-up report is being submitted to relay additional and corrected information.The following sections were updated: b4, b5, d1, g3, g6, h1, h2, h3, h6, h11.The following sections were corrected: d4, h4.No product was returned or pictures provided; visual and dimensional evaluations could not be performed.Review of the device history record identified no deviations or anomalies during manufacturing related to the reported event.A definitive root cause cannot be determined.The event cannot be confirmed.If any further information is found which would change or alter any conclusions or information, a supplemental report will be filed accordingly.Zimmer biomet will continue to monitor for trends.
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