FDA Adverse Event
Injury
Summary report: N
LUMAX 340 DR-T
MDR report key: 1020533
·
Received March 28, 2008
Report
- Report Number
- 1028232-2008-00289
- Event Type
- Injury
- Date Received
- March 28, 2008
- Date of Event
- February 15, 2008
- Report Date
- February 28, 2008
- Manufacturer
- BIOTRONIK GMBH AND CO.
- Product Code
- MRM
- PMA / PMN Number
- P00009
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- FL, US
- Reporter Occupation
- NOT APPLICABLE
Narratives
Description of Event or Problem · 1
PER MDRF, THIS SYSTEM WAS REMOVED DUE TO INFECTION. ALSO REMOVED: LINOX SD 65/16, MDR 1028232-2008-00299, SETROX S 45, MDR 1028232-2008-00311.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | LUMAX 340 DR-T | ICD | MRM | BIOTRONIK GMBH AND CO. | 355267 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Hospitalization |