ALARIS Adverse Event — Malfunction (MDR 10005000)
ALARIS Adverse Event — Malfunction (MDR 10005000) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: ALARIS; Generic name: PUMP, INFUSION, PCA; Manufacturer: CAREFUSION 303, INC..
| Device | ALARIS |
|---|---|
| Generic name | PUMP, INFUSION, PCA |
| Manufacturer | CAREFUSION 303, INC. |
| Report number | 10005000 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Narrative | PCA PUMP DISCONNECTING FROM BRAIN INTERMITTENTLY AND NOT ALARMING. THEREFORE, PATIENT PRESSING BUTTON TO RECEIVE MEDICATION AND THERE IS NO MEDICATION DISPENSING. WRITER ASSESSED PUMP AND ORDERED NEW PCA. WHEN ATTEMPTING TO RETRIEVE PATIENT HISTORY FROM PUMP FOR PCA VALUES, EACH VALUE STATED 0 (ZERO). |
| Source | openFDA MAUDE (device adverse events) |
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