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UNKNOWN CUP Adverse Event — Injury (MDR 0001825034-2020-01768)

UNKNOWN CUP Adverse Event — Injury (MDR 0001825034-2020-01768) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: UNKNOWN CUP; Generic name: PROSTHESIS, HIP; Manufacturer: ZIMMER BIOMET, INC..

DeviceUNKNOWN CUP
Generic namePROSTHESIS, HIP
ManufacturerZIMMER BIOMET, INC.
Report number0001825034-2020-01768
Event typeInjury
Product problemN
Date received2020-04-28
Report sourceDISTRIBUTOR
Narrative(B)(4). CONCOMITANT MEDICAL DEVICES: ITEM #: UNKNOWN, UNKNOWN HEAD, LOT #: UNKNOWN; ITEM #: UNKNOWN, UNKNOWN STEM, LOT #: UNKNOWN; ITEM #: UNKNOWN, UNKNOWN LINER, LOT #: UNKNOWN. AN ADDITIONAL MDR REPORT WAS FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORT: 0001825034 - 2020 - 00488. REPORTED EVENT WAS CONFIRMED BY REVIEW OF RADIOGRAPHS. DEVICE HISTORY RECORD (DHR) REVIEW WAS UNABLE TO BE PERFOR
SourceopenFDA MAUDE (device adverse events)

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