FDA Adverse Event
Malfunction
Summary report: N
UNIFY QUADRA CRT-D
MDR report key: 3210540
·
Received July 8, 2013
Report
- Report Number
- 2938836-2013-03436
- Event Type
- Malfunction
- Date Received
- July 8, 2013
- Date of Event
- May 16, 2013
- Manufacturer
- ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION
- Product Code
- NIK
- PMA / PMN Number
- P030054
- Removal / Correction Number
- NA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- NY
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
Narratives
Additional Manufacturer Narrative · 1
ALL INFORMATION PROVIDED BY MANUFACTURER, NO MEDWATCH FORM WAS RECEIVED.
Description of Event or Problem · 1
IT WAS REPORTED THAT POST-PACED T-WAVE OVERSENSING WAS OBSERVED VIA A MERLIN.NET TRANSMISSION. THE PATIENT DID NOT RECEIVE THERAPY. THE OVERSENSING WAS NOTED ON A STORED EGM. THE DEVICE WAS REPROGRAMMED AND REMAINS IMPLANTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 310668 | UNIFY QUADRA CRT-D | IMPLANTABLE CARDIOVERTER DEFIBRILLATOR | NIK | ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION | CD3249-40 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 65 YR |