FDA Adverse Event Injury Summary report: N

HEARTMATE II LVAS

MDR report key: 2983647 · Received February 28, 2013

Report

Report Number
2983647
Event Type
Injury
Date Received
February 28, 2013
Date of Event
December 20, 2012
Report Date
February 28, 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

DRIVE LINE COVER OFF REPLACED WITH CLAMSHELL BY THORATEC TECH.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
86253 HEARTMATE II LVAS LVAD DSQ THORATEC CORPORATION

Patients

Seq Age Sex Outcome Treatment
1