Additional information in h4 and h6: component, investigation type, findings, and conclusions.Device evaluation: the returned device was examined.Visual inspection revealed the tip of the device is fractured off.Potential cause: root cause was unable to be determined.This event could possibly be attributed to wear through use over time or multiple sterilization cycles.Dhr review: per dhr review, the part was likely conforming when it left zimmer biomet control.Device use this device is used for treatment.If additional information is obtained that adds value to the relevant content of this report, a follow-up report will be sent.
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