O-ARM 1000 IMAGING SYSTEM THIRD EDITION Adverse Event — Malfunction (MDR 3004785967-2020-00501)
O-ARM 1000 IMAGING SYSTEM THIRD EDITION Adverse Event — Malfunction (MDR 3004785967-2020-00501) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: O-ARM 1000 IMAGING SYSTEM THIRD EDITION; Generic name: IMAGE-INTENSIFIED FLUOROSCOPIC X-RAY SYSTEM, MOBILE; Manufacturer: MEDTRONIC NAV
| Device | O-ARM 1000 IMAGING SYSTEM THIRD EDITION |
|---|---|
| Generic name | IMAGE-INTENSIFIED FLUOROSCOPIC X-RAY SYSTEM, MOBILE |
| Manufacturer | MEDTRONIC NAVIGATION, INC (LITTLETON) |
| Report number | 3004785967-2020-00501 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | FOREIGN, HEALTH PROFESSIONAL |
| Narrative | NO PATIENT INFORMATION PROVIDED AS NO PATIENT WAS INVOLVED IN THIS CONCERN. H3,H6) 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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