IAB: 7 FR 30CC Adverse Event — Malfunction (MDR 1219856-2008-00055)
IAB: 7 FR 30CC Adverse Event — Malfunction (MDR 1219856-2008-00055) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: IAB: 7 FR 30CC; Generic name: INTRA-AORTIC BALLOON PRODUCTS; Manufacturer: ARROW INTL., INC..
| Device | IAB: 7 FR 30CC |
|---|---|
| Generic name | INTRA-AORTIC BALLOON PRODUCTS |
| Manufacturer | ARROW INTL., INC. |
| Report number | 1219856-2008-00055 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-02-15 |
| Report source | Health Professional, HEALTH PROFESSIONAL |
| Source | openFDA MAUDE (device adverse events) |
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