MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2020-03-23 for O2 BI70002000 manufactured by Medtronic Navigation, Inc (littleton).
[184470683]
No patient information provided as no patient was involved in this concern. Other relevant device(s) are: product id: bi71000823, serial/lot #: (b)(4). Product id: bi71000181, serial/lot #: (b)(4). Product id: bi71000186, serial/lot #: (b)(4). The manufacturer representative went to the site to test the imaging system. The reported issue was confirmed and they troubleshot the issue and determined it was being caused by one of the mobile view station (mvs) components. They replaced the mvs power board, mvs computer and mvs uninterruptible power supply (ups). After replacement the issue was resolved. A new mac address was added to the hospital network. The system was tested and was working properly. The computer, pcba board and power supply was returned to the manufacture for evaluation and is under analysis at this time. If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10
[184470684]
Medtronic received information regarding an imaging system. It was reported outside of a procedure that the mobile view station (mvs) will not fully boot. It gets stuck on the startup screen, then it won't shut down, even if they try to hard shut it off. They ultimately have to unplug it and wait for it to die to get it powered back down. No patient was present at the time of the event.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 3004785967-2020-00387 |
| MDR Report Key | 9865223 |
| Report Source | HEALTH PROFESSIONAL |
| Date Received | 2020-03-23 |
| Date of Report | 2020-03-23 |
| Date of Event | 2020-03-10 |
| Date Mfgr Received | 2020-03-10 |
| Device Manufacturer Date | 2016-04-26 |
| Date Added to Maude | 2020-03-23 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | STACY RUEMPING |
| Manufacturer Street | 7000 CENTRAL AVENUE NE RCW215 |
| Manufacturer City | MINNEAPOLIS MN 55432 |
| Manufacturer Country | US |
| Manufacturer Postal | 55432 |
| Manufacturer Phone | 7635260594 |
| Manufacturer G1 | MEDTRONIC NAVIGATION, INC (LITTLETON) |
| Manufacturer Street | 300 FOSTER ST |
| Manufacturer City | LITTLETON MA 01460 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 01460 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | O2 |
| Generic Name | INTERVENTIONAL FLUOROSCOPIC X-RAY SYSTEM |
| Product Code | OWB |
| Date Received | 2020-03-23 |
| Returned To Mfg | 2020-03-16 |
| Model Number | BI70002000 |
| Catalog Number | BI70002000 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | R |
| Device Eval'ed by Mfgr | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | MEDTRONIC NAVIGATION, INC (LITTLETON) |
| Manufacturer Address | 300 FOSTER ST LITTLETON MA 01460 US 01460 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2020-03-23 |