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 2018-10-30 for TRANSVENOUS LEAD 401652 manufactured by Mpri.
[125495076]
If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10
[125495077]
It was reported that the implantable pulse generator (ipg) and leads were removed due to infection. The system will be replaced in the future. No further patient complications have been reported as a result of this event.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 2649622-2018-17698 |
MDR Report Key | 8019898 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2018-10-30 |
Date of Report | 2018-10-30 |
Date of Event | 2018-10-02 |
Date Mfgr Received | 2018-10-02 |
Date Added to Maude | 2018-10-30 |
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 | ANNE SCHILLING |
Manufacturer Street | 8200 CORAL SEA ST NE |
Manufacturer City | MOUNDS VIEW MN 55112 |
Manufacturer Country | US |
Manufacturer Postal | 55112 |
Manufacturer Phone | 7635052036 |
Manufacturer G1 | MPRI |
Manufacturer Street | ROAD 149 KM 56.3 |
Manufacturer City | VILLALBA PR 00766 |
Manufacturer Country | US |
Manufacturer Postal Code | 00766 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | TRANSVENOUS LEAD |
Generic Name | ADAPTOR, LEAD, PACEMAKER |
Product Code | DTD |
Date Received | 2018-10-30 |
Model Number | 401652 |
Catalog Number | 401652 |
Operator | LAY USER/PATIENT |
Device Availability | N |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | MPRI |
Manufacturer Address | ROAD 149 KM 56.3 VILLALBA PR 00766 US 00766 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Hospitalization; 2. Required No Informationntervention | 2018-10-30 |