FDA Adverse Event Injury Summary report: N

TELEMETRY MONITORING SYSTEM

MDR report key: 51507 · Received November 18, 1996

Report

Report Number
MW4001713
Event Type
Injury
Date Received
November 18, 1996
Date of Event
December 29, 1995
Report Date
January 31, 1996
Manufacturer
SIEMENS MEDICAL SYSTEMS, INC. ELECTROMEDICAL GRP
Product Code
DRG
Adverse Event
Yes
Report Source
Voluntary report
Reporter Location
NJ, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

A VISITOR TO THE TELEMETRY UNIT WAS STANDING UNDER THE ANTENNAE OR THE TELEMETRY CENTRAL STATION WITH A CELLULAR PHONE IN THE "ON" POSITION BUT NOT MODULATING. DISTORTION WAS NOTED ON FOUR (4) FREQUENCIES ON THE CARDIAC MONITORING SYSTEM. WHEN THE SOURCE OF THE INTERFERENCE WAS DISCOVERED, THE CELLULAR PHONE WAS TURNED OFF AND THE DISTORTION CEASED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TELEMETRY MONITORING SYSTEM TELEMETRY MONITORING SYSTEM DRG SIEMENS MEDICAL SYSTEMS, INC. ELECTROMEDICAL GRP 4561 *

Patients

Seq Age Sex Outcome Treatment
1 NA Other| R