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..
| Device | UNKNOWN CUP |
|---|---|
| Generic name | PROSTHESIS, HIP |
| Manufacturer | ZIMMER BIOMET, INC. |
| Report number | 0001825034-2020-01768 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-28 |
| Report source | DISTRIBUTOR |
| 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 |
| Source | openFDA MAUDE (device adverse events) |
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