MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2019-12-26 for ENSITE VELOCITY? SYSTEM MEDIA CONVERTER Velocity? EE3000 manufactured by St. Jude Medical, Inc..
[173300344]
The results/method and conclusion codes along with investigation results will be provided in the final report further information regarding the event were requested but not received.
Patient Sequence No: 1, Text Type: N, H10
[173300345]
During the procedure, the dws computer could not boot to login screen. All the usb devices were disconnected with no resolution. Further troubleshooting revealed the issue was due to the digital converter. The patient was prepped and the procedure was cancelled with no patient consequences.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 2184149-2019-00255 |
MDR Report Key | 9521611 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2019-12-26 |
Date of Report | 2020-03-03 |
Date of Event | 2019-12-06 |
Date Mfgr Received | 2020-02-06 |
Date Added to Maude | 2019-12-26 |
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 | STEPHANIE O' SULLIVAN |
Manufacturer Street | 5050 NATHAN LANE NORTH |
Manufacturer City | PLYMOUTH MN 55442 |
Manufacturer Country | US |
Manufacturer Postal | 55442 |
Manufacturer Phone | 6517565400 |
Manufacturer G1 | ST. JUDE MEDICAL, INC. (AF-ST. PAUL) |
Manufacturer Street | ONE ST. JUDE MEDICAL DRIVE |
Manufacturer City | ST. PAUL MN 55117 |
Manufacturer Country | US |
Manufacturer Postal Code | 55117 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | ENSITE VELOCITY? SYSTEM MEDIA CONVERTER |
Generic Name | COMPUTER, DIAGNOSTIC, PROGRAMMABLE |
Product Code | DQK |
Date Received | 2019-12-26 |
Model Number | Velocity? |
Catalog Number | EE3000 |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ST. JUDE MEDICAL, INC. |
Manufacturer Address | ONE ST. JUDE MEDICAL DRIVE ST. PAUL MN 55117 US 55117 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-12-26 |