CVC SET: 22 GA X 4 Adverse Event — Malfunction (MDR 1036844-2008-00015)
CVC SET: 22 GA X 4 Adverse Event — Malfunction (MDR 1036844-2008-00015) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: CVC SET: 22 GA X 4; Generic name: SINGLE LUMEN CVC PRODUCTS; Manufacturer: ARROW INTL., INC..
| Device | CVC SET: 22 GA X 4 |
|---|---|
| Generic name | SINGLE LUMEN CVC PRODUCTS |
| Manufacturer | ARROW INTL., INC. |
| Report number | 1036844-2008-00015 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-02-15 |
| Report source | Foreign, User facility |
| Narrative | IT WAS REPORTED THAT UPON A SECOND ATTEMPT, THE PHYSICIAN INTRODUCED THE GUIDEWIRE; HOWEVER, THE PHYSICIAN FOUND IT IMPOSSIBLE TO REMOVE THE NEEDLE. THE NEEDLE APPEARED TO BE BROKEN ON THE GUIDEWIRE. AS A RESULT, THE PHYSICIAN REMOVED THE NEEDLE AND THE GUIDEWIRE SIMULTANEOUSLY. THERE WERE NO PT COMPLICATIONS REPORTED. |
| Source | openFDA MAUDE (device adverse events) |
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