BD NEXIVA¿ CLOSED IV CATHETER SYSTEM Adverse Event — Malfunction (MDR 1710034-2020-00274)
BD NEXIVA¿ CLOSED IV CATHETER SYSTEM Adverse Event — Malfunction (MDR 1710034-2020-00274) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: BD NEXIVA¿ CLOSED IV CATHETER SYSTEM; Generic name: INTRAVASCULAR CATHETER; Manufacturer: BECTON DICKINSON INFUSION THERAPY SYSTEMS INC..
| Device | BD NEXIVA¿ CLOSED IV CATHETER SYSTEM |
|---|---|
| Generic name | INTRAVASCULAR CATHETER |
| Manufacturer | BECTON DICKINSON INFUSION THERAPY SYSTEMS INC. |
| Report number | 1710034-2020-00274 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | FOREIGN, OTHER, USER FACILITY |
| Narrative | H.6. INVESTIGATION SUMMARY: OUR QUALITY ENGINEER INSPECTED THE PHOTOGRAPHS SUBMITTED FOR EVALUATION. BD RECEIVED THREE PHOTOGRAPHS. FROM THE REPORTED DESCRIPTION, IT STATES THAT LEAKAGE WAS OBSERVED AT THE BASE OF THE CATHETER TUBING/NOSE OF THE ADAPTER. FURTHER INSPECTION OF THE RECEIVED PHOTOS REVEALS SOME POTENTIAL MEDIA ON THE OUTSIDE OF THE CATHETER TUBING HOWEVER IT CANNOT BE DETERMINED WITH |
| Source | openFDA MAUDE (device adverse events) |
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