An investigation report from an implant retrieval center was received and reported that during examination of the rod, the retrieval center found that the rod was fractured.Additionally, there was a locking pin failure, corrosion, wear, scratches, and other surface damage was noted and the rod was unable to be distracted.It was reported that the rod was removed as part of a planned removal procedure; there was no adverse patient or user impact associated with this report.No additional information is available.Report 2 of 2.
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