CALAXO SCREW Adverse Event — Malfunction (MDR 1219602-2008-00038)
CALAXO SCREW Adverse Event — Malfunction (MDR 1219602-2008-00038) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: CALAXO SCREW; Generic name: CALAXO; Manufacturer: SMITH & NEPHEW INC. ENDOSCOPY DIVISION.
| Device | CALAXO SCREW |
|---|---|
| Generic name | CALAXO |
| Manufacturer | SMITH & NEPHEW INC. ENDOSCOPY DIVISION |
| Report number | 1219602-2008-00038 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-02-14 |
| Report source | Consumer, Company representation |
| Narrative | PATIENT HAS HAD A REACTION OF THE SCREW AND REPORTS INFLAMMATION AND PAIN OVER THE SITE. |
| Source | openFDA MAUDE (device adverse events) |
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