* Adverse Event — Malfunction (MDR 9616240-2007-00118)
* Adverse Event — Malfunction (MDR 9616240-2007-00118) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: *; Generic name: *; Manufacturer: *.
| Device | * |
|---|---|
| Generic name | * |
| Manufacturer | * |
| Report number | 9616240-2007-00118 |
| Event type | Malfunction |
| Product problem | * |
| Date received | 2007-12-19 |
| Report source | Health Professional, User facility, Company representation |
| Narrative | IMPROVEMENTS TO INCREASE THE ROBUSTNESS OF THE HYDRAULIC CONNECTIONS HAVE BEEN DESIGNED AND VALIDATED AND ARE CURRENTLY BEING INTRODUCED IN THE FIELD TO AVOID THE OCCURRENCE OF TUBING DISCONNECTION. |
| Source | openFDA MAUDE (device adverse events) |
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