FDA Adverse Event
Malfunction
Summary report: N
54 CM BIPOLAR LEAD
MDR report key: 3243101
·
Received July 18, 2013
Report
- Report Number
- 2183787-2013-00062
- Event Type
- Malfunction
- Date Received
- July 18, 2013
- Report Date
- July 12, 2013
- Manufacturer
- GREATBATCH MEDICAL
- Product Code
- DTB
- PMA / PMN Number
- P130012
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CA, US
- Reporter Occupation
- NOT APPLICABLE
Narratives
Description of Event or Problem · 1
THE LEAD WAS CAPPED DUE TO NON-CAPTURE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 336596 | 54 CM BIPOLAR LEAD | BIPOLAR LEAD | DTB | GREATBATCH MEDICAL | 511212 | W2340235 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Required Intervention |