O2 Adverse Event — Malfunction (MDR 3004785967-2020-00502)
O2 Adverse Event — Malfunction (MDR 3004785967-2020-00502) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: O2; Generic name: INTERVENTIONAL FLUOROSCOPIC X-RAY SYSTEM; Manufacturer: MEDTRONIC NAVIGATION, INC (LITTLETON).
| Device | O2 |
|---|---|
| Generic name | INTERVENTIONAL FLUOROSCOPIC X-RAY SYSTEM |
| Manufacturer | MEDTRONIC NAVIGATION, INC (LITTLETON) |
| Report number | 3004785967-2020-00502 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | COMPANY REPRESENTATIVE, FOREIG |
| Narrative | OTHER RELEVANT DEVICE(S) ARE: PRODUCT ID: BI71000450, LOT/SERIAL #: UNKNOWN, FOREIGN COUNTRY: (B)(6). NO PARTS HAVE BEEN RECEIVED BY THE MANUFACTURER FOR EVALUATION. IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED. |
| Source | openFDA MAUDE (device adverse events) |
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