Medical device Adverse Event — Malfunction (MDR 8010042-2008-00009)
Medical device Adverse Event — Malfunction (MDR 8010042-2008-00009) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Report number: 8010042-2008-00009; Event type: Malfunction; Date received: 2008-01-23.
| Report number | 8010042-2008-00009 |
|---|---|
| Event type | Malfunction |
| Date received | 2008-01-23 |
| Report source | Foreign, Health Professional, User facility, Company representation |
| Narrative | MAQUET INC. SUBMITS THIS REPORT ON BEHALF OF THE DEVICE MFG FACILITY. MAQUET CRITICAL CARE AB PROVIDES PRODUCT FAILURE INVESTIGATION, ANALYSIS AND RESOLUTION FOR THE DEVICE DESCRIBED IN THIS REPORT. |
| Source | openFDA MAUDE (device adverse events) |
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