(b)(4).Multiple mdr reports were filed for this event.Please see associated reports: 0001825034 - 2018 - 01409, 0001825034 - 2018 - 01410, 0001825034 - 2018 - 01411, 0001825034 - 2018 - 01412, 0001825034 - 2018 - 01413, 0001825034 - 2018 - 01415.Concomitant medical products: 211224 compr srs ic seg - 30mm, unknown lot, 211237 compr srs mod stem - 10x100mm, unknown lot, 211253 compr srs 50mm dst hml bdy rt, unknown lot, unknown part/lot; proximal body, regenerx augment, seas augment.Report source: foreign.The event occurred in the (b)(6).Reported event was unable to be confirmed as part number / lot number of device involved in the incident is unknown.Device history record (dhr) review was unable to be performed as the lot number of the device involved in the event is unknown.Root cause was unable to be determined as the necessary information to adequately investigate the reported event was not provided.If any further information is found which would change or alter any conclusions or information, a supplemental will be filed accordingly.Zimmer biomet will continue to monitor for trends.This report is being submitted late as it has been identified in remediation.Device remains implanted.
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It was reported that the patient found it severely difficult to open jar, do heavy chores, carry bag, wash back, cut grass, perform social activities, and perform daily activities.The patient experienced moderate pain and moderate tingling.Attempts have been made and no further information has been made available at this time.
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