BD POSIFLUSH¿ SYRINGE Adverse Event — Malfunction (MDR 1911916-2020-00415)
BD POSIFLUSH¿ SYRINGE Adverse Event — Malfunction (MDR 1911916-2020-00415) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: BD POSIFLUSH¿ SYRINGE; Generic name: SALINE VASCULAR ACCESS FLUSH; Manufacturer: BD MEDICAL (BD WEST) MEDICAL SURGICAL.
| Device | BD POSIFLUSH¿ SYRINGE |
|---|---|
| Generic name | SALINE VASCULAR ACCESS FLUSH |
| Manufacturer | BD MEDICAL (BD WEST) MEDICAL SURGICAL |
| Report number | 1911916-2020-00415 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | FOREIGN, OTHER, USER FACILITY |
| Narrative | INVESTIGATION SUMMARY: TWO PHOTOS WERE PROVIDED. ONE PHOTO SHOW TWO SYRINGES. BOTH ARE WITH NO PACKAGING FLOW WRAP, DO NOT HAVE TIP CAP NOR SALINE SOLUTION. ONE SAMPLE HAS THE PLUNGER ROD-RUBBER STOPPER ALL THE WAY DOWN. THE OTHER SYRINGE HAS THE PLUNGER ROD-RUBBER STOPPER ALL THE WAY UP WHICH HAS ALREADY OVER THE RETENTION RING, THIS POSITION IS NOT HOW IT THE SYRINGE IS PRODUCED. THE OTHER PHOTO |
| Source | openFDA MAUDE (device adverse events) |
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