Corrections: h3 additional information: h6, component codes, type of investigations, findings, conclusions.Device evaluation: visual inspection revealed all six returned devices have damaged threads.Potential cause.Root cause was unable to be determined.This event could possibly be attributed to cross threading during use.Dhr review.Per dhr review, the part was likely conforming when it left zimmer biomet control.Device usage.This device is used for treatment.A follow-up report will be submitted if new information is received that changes the information provided in this report.
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