PRIMARY PLUM SET, CLAVE PORT, CLAVE Y-SITE Adverse Event — Malfunction (MDR 10000321)
PRIMARY PLUM SET, CLAVE PORT, CLAVE Y-SITE Adverse Event — Malfunction (MDR 10000321) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: PRIMARY PLUM SET, CLAVE PORT, CLAVE Y-SITE; Generic name: SET, ADMINISTRATION, INTRAVASCULAR; Manufacturer: HOSPIRA, INC..
| Device | PRIMARY PLUM SET, CLAVE PORT, CLAVE Y-SITE |
|---|---|
| Generic name | SET, ADMINISTRATION, INTRAVASCULAR |
| Manufacturer | HOSPIRA, INC. |
| Report number | 10000321 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Narrative | TUBING LEFT IN OFFICE WITH NOTE "SOMETHING WRONG WITH PRIMING PLUNGER." TUBING AND PACKING AVAILABLE FOR REVIEW IF NEEDED. LOT #434909. |
| Source | openFDA MAUDE (device adverse events) |
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