MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2020-03-31 for MAIN CART 9735669 STEALTH S8 EM ENT manufactured by Medtronic Navigation, Inc.
[185949603]
No patient involved. Other relevant device(s) are: product id: 9735736, software version: (b)(4). No devices were returned to the manufacturer for analysis. If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10
[185949604]
Medtronic received information regarding a navigation system used outside of procedure. It was reported that the system was booting into error screen. Troubleshooting included using ctrl+alt+del we were able to get to the grub menu and fix, allowing the system to boot to login screen. No patient present.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1723170-2020-01107 |
MDR Report Key | 9902674 |
Report Source | COMPANY REPRESENTATIVE |
Date Received | 2020-03-31 |
Date of Report | 2020-03-31 |
Date of Event | 2020-03-11 |
Date Mfgr Received | 2020-03-11 |
Device Manufacturer Date | 2019-01-22 |
Date Added to Maude | 2020-03-31 |
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 |
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 |
Manufacturer Street | 826 COAL CREEK CIRCLE |
Manufacturer City | LOUISVILLE CO 80027 |
Manufacturer Country | US |
Manufacturer Postal Code | 80027 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | MAIN CART 9735669 STEALTH S8 EM ENT |
Generic Name | INSTRUMENT, STEREOTAXIC |
Product Code | HAW |
Date Received | 2020-03-31 |
Model Number | 9735669 |
Catalog Number | 9735669 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | MEDTRONIC NAVIGATION, INC |
Manufacturer Address | 826 COAL CREEK CIRCLE LOUISVILLE CO 80027 US 80027 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-31 |