MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,consum report with the FDA on 2020-03-10 for VALITUDE X4 CRT-P U128 manufactured by Boston Scientific Corporation.
[182720051]
As no further information concerning this report is expected, our investigation is complete. This investigation will be updated should further information be provided.
Patient Sequence No: 1, Text Type: N, H10
[182720052]
It was reported that this cardiac resynchronization therapy pacemaker (crt-p) was part of a system revision due to infection with sepsis. Additional information received indicates that this crt-p was explanted and was used as an external temporary pacemaker. The patient was treated with intravenous antibiotics. There were no additional adverse patient effects reported. The crt-p was explanted.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 2124215-2020-05184 |
MDR Report Key | 9811136 |
Report Source | COMPANY REPRESENTATIVE,CONSUM |
Date Received | 2020-03-10 |
Date of Report | 2020-03-19 |
Date of Event | 2020-01-13 |
Date Mfgr Received | 2020-02-19 |
Device Manufacturer Date | 2018-05-29 |
Date Added to Maude | 2020-03-10 |
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 | TIMOTHY DEGROOT |
Manufacturer Street | 4100 HAMLINE AVENUE NORTH |
Manufacturer City | SAINT PAUL MN 55112 |
Manufacturer Country | US |
Manufacturer Postal | 55112 |
Manufacturer Phone | 6515826168 |
Manufacturer G1 | BOSTON SCIENTIFIC CORPORATION |
Manufacturer Street | CASHEL ROAD |
Manufacturer City | CLONMEL |
Manufacturer Country | EI |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | VALITUDE X4 CRT-P |
Generic Name | PULSE GENERATOR, PACEMAKER, IMPLANTABLE, WITH CARDIAC RESYNCHRONIZATION (CRT-P) |
Product Code | NKE |
Date Received | 2020-03-10 |
Model Number | U128 |
Catalog Number | U128 |
Lot Number | 732063 |
Operator | LAY USER/PATIENT |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | BOSTON SCIENTIFIC CORPORATION |
Manufacturer Address | 4100 HAMLINE AVENUE NORTH SAINT PAUL MN 55112 US 55112 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Death; 2. Hospitalization; 3. Life Threatening; 4. Required No Informationntervention | 2020-03-10 |