FDA Adverse Event Death Summary report: N

DLP PERFUSION ADAPTOR

MDR report key: 1634848 · Received March 16, 2010

Report

Report Number
1634848
Event Type
Death
Date Received
March 16, 2010
Date of Event
December 24, 2009
Report Date
March 16, 2010
Manufacturer
MEDTRONIC
Product Code
DTL
Adverse Event
Yes
Report Source
User Facility report
Reporter Location
IL, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

WHILE MOVING PATIENT FOR BASIC NURSING CARE, ADAPTOR SNAPPED. PATIENT STARTED TO BLEED FROM CATHETERS AS A RESULT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 DLP PERFUSION ADAPTOR ADAPTOR, CARDIOPULMONARY BYPASS DTL MEDTRONIC * UNK

Patients

Seq Age Sex Outcome Treatment
1 39 YR Death CARDIAC DRUGS| LONG-TERM ANTIBIOTICS