ENTERALITE INFINITY ENTERAL INFUSION PUMP Adverse Event — Malfunction (MDR 1722139-2020-00151)
ENTERALITE INFINITY ENTERAL INFUSION PUMP Adverse Event — Malfunction (MDR 1722139-2020-00151) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: ENTERALITE INFINITY ENTERAL INFUSION PUMP; Generic name: ENTERAL INFUSION PUMP; Manufacturer: MOOG MEDICAL DEVICES GROUP.
| Device | ENTERALITE INFINITY ENTERAL INFUSION PUMP |
|---|---|
| Generic name | ENTERAL INFUSION PUMP |
| Manufacturer | MOOG MEDICAL DEVICES GROUP |
| Report number | 1722139-2020-00151 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | USER FACILITY |
| Narrative | THIS DEVICE WAS NOT RETURNED TO MMDG FOR EVALUATION. A DHR REVIEW WAS COMPLETED AND FOUND NO NON-CONFORMANCES ASSOCIATED WITH THE DEVICE. BECAUSE THE PUMP WAS NOT RETURNED, MMDG WAS UNABLE TO INVESTIGATE THE COMPLAINT. THIS REPORT IS BEING FILED BECAUSE THE EVENT OCCURRED WHILE THE DEVICE WAS IN USE BY A PEDIATRIC PATIENT. PER OUR PROCEDURES ALL REPORTS OF THIS TYPE OF EVENT THAT INVOLVE A PEDIATR |
| Source | openFDA MAUDE (device adverse events) |
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