IMHS Adverse Event — Injury (MDR 1020279-2008-00052)
IMHS Adverse Event — Injury (MDR 1020279-2008-00052) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: IMHS; Generic name: INTERNAL FIXATION - NAIL; Manufacturer: SMITH & NEPHEW, INC., ORTHOPAEDIC DIV..
| Device | IMHS |
|---|---|
| Generic name | INTERNAL FIXATION - NAIL |
| Manufacturer | SMITH & NEPHEW, INC., ORTHOPAEDIC DIV. |
| Report number | 1020279-2008-00052 |
| Event type | Injury |
| Product problem | N |
| Date received | 2008-02-19 |
| Report source | Company representation |
| Narrative | PT UNDERWENT EXTENDED SURGERY TIME DUE TO THE END CAP COULD NOT BE INSERTED DURING SURGERY. |
| Source | openFDA MAUDE (device adverse events) |
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