FDA Adverse Event
Injury
Summary report: N
HEARTMATE II LVAS
MDR report key: 1914529
·
Received December 3, 2010
Report
- Report Number
- 1914529
- Event Type
- Injury
- Date Received
- December 3, 2010
- Date of Event
- September 28, 2009
- Report Date
- April 20, 2011
- Manufacturer
- THORATEC CORPORATION
- Product Code
- DSQ
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- User Facility report
- Reporter Location
- AL, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
MAJOR PUMP UNIT(S) INVOLVED: BLOOD PUMPADDITIONAL TEXT: INFLOW TO PUMP STENOSEDSPECIFIC COMPONENT(S) INVOLVED: INFLOW GRAFT MALFUNCTION/MALPOSITIONADDITIONAL TEXT: STENOSEDOTHER COMPONENT:CAUSATIVE OR CONTRIBUTING FACTOR: NO SPECIFIC CONTRIBUTING CAUSE IDENTIFIEDOTHER CAUSE:INTERVENTION(S): REPLACEMENT OF INFLOW GRAFT; REPLACEMENT OF PUMPOTHER INTERVENTION :IMPLANT DEVICE TYPE: LVADMALFUNCTION DEVICE TYPE:
Description of Event or Problem · 1
MAJOR PUMP UNIT(S) INVOLVED: BLOOD PUMP.SPECIFIC COMPONENT(S) INVOLVED: INFLOW GRAFT MALFUNCTION/MALPOSITION.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | HEARTMATE II LVAS | LVAD | DSQ | THORATEC CORPORATION |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 51.3 YR |