UNKNOWN DRILL Adverse Event — Malfunction (MDR 1020279-2020-01389)
UNKNOWN DRILL Adverse Event — Malfunction (MDR 1020279-2020-01389) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: UNKNOWN DRILL; Generic name: GUIDE, SURGICAL, INSTRUMENT; Manufacturer: SMITH & NEPHEW, INC..
| Device | UNKNOWN DRILL |
|---|---|
| Generic name | GUIDE, SURGICAL, INSTRUMENT |
| Manufacturer | SMITH & NEPHEW, INC. |
| Report number | 1020279-2020-01389 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | COMPANY REPRESENTATIVE, USER F |
| Narrative | IT WAS REPORTED THAT DURING SURGERY, DRILL COLD WELD INSIDE OF A DRILL GUIDE. NO INJURY WAS REPORTED. IT IS UNKNOWN IF THERE WAS A DELAY OR HOW WAS THE PROCEDURE CONCLUDED. |
| Source | openFDA MAUDE (device adverse events) |
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