FDA Adverse Event
Death
Summary report: N
HEARTMATE II LVAS
MDR report key: 3173771
·
Received June 17, 2013
Report
- Report Number
- 3173771
- Event Type
- Death
- Date Received
- June 17, 2013
- Date of Event
- June 12, 2013
- Report Date
- June 17, 2013
- Manufacturer
- THORATEC CORPORATION
- Product Code
- DSQ
- Adverse Event
- Yes
- Report Source
- User Facility report
- Reporter Location
- AL, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
PATIENT CUT DRIVELINE WITH SCISSORS WHILE CHANGING HIS DIAPER.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 273933 | HEARTMATE II LVAS | LVAD | DSQ | THORATEC CORPORATION | * | * |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | * | Death |