28MM DIA COCR MOD HD -3MM NK Adverse Event — Injury (MDR 0001825034-2020-01807)
28MM DIA COCR MOD HD -3MM NK Adverse Event — Injury (MDR 0001825034-2020-01807) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: 28MM DIA COCR MOD HD -3MM NK; Generic name: PROSTHESIS, HIP; Manufacturer: ZIMMER BIOMET, INC..
| Device | 28MM DIA COCR MOD HD -3MM NK |
|---|---|
| Generic name | PROSTHESIS, HIP |
| Manufacturer | ZIMMER BIOMET, INC. |
| Report number | 0001825034-2020-01807 |
| Event type | Injury |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | COMPANY REPRESENTATIVE, DISTRI |
| Narrative | NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT. |
| Source | openFDA MAUDE (device adverse events) |
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