VESSEL CATH KIT: 24 GA X 3-1/2 Adverse Event — Malfunction (MDR 1036844-2008-00011)
VESSEL CATH KIT: 24 GA X 3-1/2 Adverse Event — Malfunction (MDR 1036844-2008-00011) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: VESSEL CATH KIT: 24 GA X 3-1/2; Generic name: SINGLE LUMEN CVC PRODUCTS; Manufacturer: ARROW INTL., INC..
| Device | VESSEL CATH KIT: 24 GA X 3-1/2 |
|---|---|
| Generic name | SINGLE LUMEN CVC PRODUCTS |
| Manufacturer | ARROW INTL., INC. |
| Report number | 1036844-2008-00011 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-02-15 |
| Report source | Foreign, Health Professional |
| Narrative | IT WAS REPORTED, BY THE CUSTOMER, AFTER SEVERAL ATTEMPTS TO PLACE THE SPRING WIRE GUIDE (SWG) IN A NEW BORN BABY WITH OESOPHAGEAL ATRESIA, THE SWG BECAME UNRAVELED. AS A RESULT, THE PHYSICIAN SUCCESSFULLY PERFORMED A SWG EXCHANGE AND THE CATHETER WAS PLACED. THERE WRE NO PT COMPLICATIONS REPORTED. |
| Source | openFDA MAUDE (device adverse events) |
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