MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2020-03-31 for CLARIA MRI QUAD CRT-D SURESCAN DTMA2QQ manufactured by Medtronic Europe Sarl.
[185763345]
If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10
[185763346]
It was reported that the day after the implant, the left ventricular (lv) lead was found to be dislodged and exhibited pacing failure. The cardiac resynchronization therapy defibrillator (crt-d) device had also moved downward five centimeters. The lv lead was repositioned and the crt-d was sutured deeper into the tissue and was stable. No patient complications have been reported as a result of this event.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 9614453-2020-01119 |
MDR Report Key | 9903617 |
Report Source | COMPANY REPRESENTATIVE,FOREIG |
Date Received | 2020-03-31 |
Date of Report | 2020-03-31 |
Date of Event | 2020-03-12 |
Date Mfgr Received | 2020-03-12 |
Device Manufacturer Date | 2019-12-12 |
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 | PAULA BIXBY |
Manufacturer Street | 8200 CORAL SEA ST NE |
Manufacturer City | MOUNDS VIEW MN 55112 |
Manufacturer Country | US |
Manufacturer Postal | 55112 |
Manufacturer Phone | 7635055378 |
Manufacturer G1 | MEDTRONIC EUROPE SARL |
Manufacturer Street | ROUTE DU MOLLIAU 31 CASE POSTALE |
Manufacturer City | TOLOCHENAZ VAUD 1131 |
Manufacturer Country | CH |
Manufacturer Postal Code | 1131 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | CLARIA MRI QUAD CRT-D SURESCAN |
Generic Name | DEFIBRILLATOR, AUTOMATIC IMPLANTABLE CARDIOVERTER, WITH CARDIAC RESYNCHRONIZATIO |
Product Code | NIK |
Date Received | 2020-03-31 |
Model Number | DTMA2QQ |
Catalog Number | DTMA2QQ |
Operator | LAY USER/PATIENT |
Device Availability | N |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | MEDTRONIC EUROPE SARL |
Manufacturer Address | ROUTE DU MOLLIAU 31 CASE POSTALE TOLOCHENAZ VAUD 1131 CH 1131 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 439878 | 1. Hospitalization; 2. Required No Informationntervention | 2020-03-31 |