CADD-LEGACY DUODOPA AMBULATORY INFUSION PUMP Adverse Event — Malfunction (MDR 3012307300-2020-03451)
CADD-LEGACY DUODOPA AMBULATORY INFUSION PUMP Adverse Event — Malfunction (MDR 3012307300-2020-03451) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: CADD-LEGACY DUODOPA AMBULATORY INFUSION PUMP; Generic name: PUMP, INFUSION, ENTERAL; Manufacturer: SMITHS MEDICAL ASD, INC..
| Device | CADD-LEGACY DUODOPA AMBULATORY INFUSION PUMP |
|---|---|
| Generic name | PUMP, INFUSION, ENTERAL |
| Manufacturer | SMITHS MEDICAL ASD, INC. |
| Report number | 3012307300-2020-03451 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | DISTRIBUTOR |
| Narrative | INFORMATION WAS RECEIVED INDICATING THAT A SMITHS MEDICAL CADD-LEGACY DUODOPA AMBULATORY INFUSION PUMP WAS SET TO 4.3 INSTEAD OF 4.1. PER REPORTER IT WAS A "HANDLING ERROR." IT WAS REPORTED THAT THE PATIENT WAS HOSPITALIZED IN (B)(6) SINCE LAST NIGHT FOR COVID19 SUSPICION AND HALLUCINATIONS. NO ADDITIONAL ADVERSE EFFECTS WERE REPORTED. |
| Source | openFDA MAUDE (device adverse events) |
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