EMBRACE PUMP Adverse Event — Malfunction (MDR 1527460-2008-00143)
EMBRACE PUMP Adverse Event — Malfunction (MDR 1527460-2008-00143) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: EMBRACE PUMP; Generic name: 80 LZH PUMP, INFUSION, ENTERAL; Manufacturer: ROSS PRODUCTS DIVISION.
| Device | EMBRACE PUMP |
|---|---|
| Generic name | 80 LZH PUMP, INFUSION, ENTERAL |
| Manufacturer | ROSS PRODUCTS DIVISION |
| Report number | 1527460-2008-00143 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-02-18 |
| Report source | Other, Company representation |
| Narrative | CRACKED OR BROKEN PIVOT POINT. |
| Source | openFDA MAUDE (device adverse events) |
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