(b)(4).Reported event was unable to be confirmed due to limited information received from the customer.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 with the information 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.Unique identifier (udi) #: n/a.Concomitant medical products: item # 51-109080, tloc 133 mp sp t1 pps ho 8x101, lot # unk; item # 650-1057, cer bioloxd option hd 36mm, lot # unk; item # 110017102, g7 finned 3 hole shell 50d, lot # unk; item # unk, liner, lot # unk.Multiple mdr reports were filed for this event, please see associated reports: 0001825034 - 2018 - 05619; 0001825034 - 2018 - 05620; 0001825034 - 2018 - 05621; 0001825034 - 2018 - 05622.
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