CAPTURED SCREWDRIVER SHORT Adverse Event — Malfunction (MDR 0001822565-2020-01370)
CAPTURED SCREWDRIVER SHORT Adverse Event — Malfunction (MDR 0001822565-2020-01370) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: CAPTURED SCREWDRIVER SHORT; Generic name: TRAUMA INSTRUMENTATION; Manufacturer: ZIMMER BIOMET, INC..
| Device | CAPTURED SCREWDRIVER SHORT |
|---|---|
| Generic name | TRAUMA INSTRUMENTATION |
| Manufacturer | ZIMMER BIOMET, INC. |
| Report number | 0001822565-2020-01370 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | DISTRIBUTOR, FOREIGN, HEALTH PR |
| Narrative | NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT. |
| Source | openFDA MAUDE (device adverse events) |
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