FDA Adverse Event
Injury
Summary report: N
MEDTRONIC
MDR report key: 1734491
·
Received June 18, 2010
Report
- Report Number
- MW5016452
- Event Type
- Injury
- Date Received
- June 18, 2010
- Date of Event
- June 18, 2010
- Report Date
- June 18, 2010
- Manufacturer
- MEDTRONIC
- Product Code
- DXY
- Product Problem
- Yes
- Report Source
- Voluntary report
- Reporter Location
- GA, US
- Reporter Occupation
- PHYSICIAN
Narratives
Description of Event or Problem · 1
REID SWITCH FAILED TO CLOSE LEADING TO PREMATURE BATTERY DEPLETION. NO PACEMAKER DIAGNOSTIC INFORMATION COULD BE RETRIEVED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | MEDTRONIC | KAPPA | DXY | MEDTRONIC | KDR901 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 72 YR | Disability |