FDA Adverse Event
Malfunction
Summary report: N
CONSULTA CRT-D
MDR report key: 2130590
·
Received June 16, 2011
Report
- Report Number
- 6000144-2011-03348
- Event Type
- Malfunction
- Date Received
- June 16, 2011
- Date of Event
- April 23, 2011
- Manufacturer
- MEDTRONIC MED REL, INC.
- Product Code
- NIK
- PMA / PMN Number
- P010031/S084
- Removal / Correction Number
- ASKU
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CA, US
- Reporter Occupation
- PATIENT
Narratives
Additional Manufacturer Narrative · 1
THE INFORMATION SUBMITTED REFLECTS ALL RELEVANT DATA RECEIVED. IF ADDITIONAL RELEVANT INFORMATION IS RECEIVED, A SUPPLEMENTAL REPORT WILL BE SUBMITTED.
Description of Event or Problem · 1
IT WAS REPORTED BY THE PATIENT THAT THEY HEARD BEEPING FROM THE DEVICE AND IT REPEATED EVERY 6-8 HOURS SINCE THEN. THE DEVICE REMAINS IN USE. NO PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | CONSULTA CRT-D | IMPLANTABLE PACEMAKER/CARDIO/DEFIB | NIK | MEDTRONIC MED REL, INC. | D224TRK | ASKU |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 47 YR | Other | 4542 COMPETITOR IMPLANTABLE PACING LEAD| 4076 IMPLANTABLE PACING LEAD| 0184 COMPETITOR IMPLANTABLE TACHY LEAD| 4469 COMPETITOR IMPLANTABLE PACING LEAD |