CENTRAL LINE BUNDLE 7FR, 3L, 20 CM Adverse Event — Malfunction (MDR 1417592-2020-00047)
CENTRAL LINE BUNDLE 7FR, 3L, 20 CM Adverse Event — Malfunction (MDR 1417592-2020-00047) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: CENTRAL LINE BUNDLE 7FR, 3L, 20 CM; Generic name: CENTRAL LINE BUNDLE 7FR, 3L, 20 CM; Manufacturer: CENTURION MEDICAL PRODUCTS.
| Device | CENTRAL LINE BUNDLE 7FR, 3L, 20 CM |
|---|---|
| Generic name | CENTRAL LINE BUNDLE 7FR, 3L, 20 CM |
| Manufacturer | CENTURION MEDICAL PRODUCTS |
| Report number | 1417592-2020-00047 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | HEALTH PROFESSIONAL, USER FACI |
| Narrative | IT WAS REPORTED BY THE PHYSICIAN THAT THE GUIDEWIRE SPLIT AT THE CURVED TIP. THE OUTER CASING WAS REMOVED WITH THE COIL PART OF THE WIRE REMAINING IN THE BROWN PORT OF THE TRIPLE LUMEN CATHETER HOWEVER, THE MD STATES THEY WERE ABLE TO USE THE OTHER TWO PORTS OF THE LINE. THE REPORTING FACILITY HAS NOT PROVIDED AN EXACT DATE FOR THIS INCIDENT. THE REPORTING PHYSICIAN STATES, "THE PATIENT WAS CRITIC |
| Source | openFDA MAUDE (device adverse events) |
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