Review of the device history records indicate devices were manufactured and accepted into final stock with no relevant reported discrepancies.There have been no other similar events for the lot referenced.It was noted that the device is not available for evaluation.Should additional information become available, it will be provided in a supplemental report upon completion of the investigation.The information in this report was provided by stryker orthopaedics legal affairs department.No additional information is available at this time due to the ongoing litigation.Should additional information become available, the evaluation summary will be submitted in a supplemental report.The following devices were also listed in this report: unknown_joint replacement_product; cat# unk_jr; lot# unknown, triathlon pkr femur #3 lm/rl; cat# 5610-f-301; lot# wvbt, triathlon pkr baseplate #4 lm/rl; cat# 5620-b-401; lot# xhoua.It cannot be determined which, if any of these devices may have caused or contributed to the patient's experience.
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