FDA Adverse Event Injury Summary report: N

HEARTMATE II LVAS

MDR report key: 2962484 · Received February 14, 2013

Report

Report Number
2962484
Event Type
Injury
Date Received
February 14, 2013
Date of Event
April 23, 2011
Report Date
February 14, 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

TRANSIENT THROMBUS OF LVAD RESOLVED WITH ANTICOAGULATION. SUCK DOWNEVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
65410 HEARTMATE II LVAS LVAD DSQ THORATEC CORPORATION

Patients

Seq Age Sex Outcome Treatment
1