FDA Adverse Event Injury Summary report: N

MEDTRONIC

MDR report key: 1734491 · Received June 18, 2010

Report

Report Number
MW5016452
Event Type
Injury
Date Received
June 18, 2010
Date of Event
June 18, 2010
Report Date
June 18, 2010
Manufacturer
MEDTRONIC
Product Code
DXY
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
GA, US
Reporter Occupation
PHYSICIAN

Narratives

Description of Event or Problem · 1

REID SWITCH FAILED TO CLOSE LEADING TO PREMATURE BATTERY DEPLETION. NO PACEMAKER DIAGNOSTIC INFORMATION COULD BE RETRIEVED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MEDTRONIC KAPPA DXY MEDTRONIC KDR901

Patients

Seq Age Sex Outcome Treatment
1 72 YR Disability