FDA Adverse Event Injury Summary report: N

MEDTRONIC PHYSIO CONTROL

MDR report key: 312159 · Received January 10, 2001

Report

Report Number
312159
Event Type
Injury
Date Received
January 10, 2001
Date of Event
January 10, 2001
Report Date
January 10, 2001
Manufacturer
MEDTRONIC PHYSIO CONTROL
Product Code
LDD
Product Problem
Yes
Report Source
User Facility report
Reporter Location
TX, US
Reporter Occupation
PARAMEDIC

Narratives

Description of Event or Problem · 1

AT SCENE FOUND PT WITH NO PULSE OR RESPIRATIONS. ATTACHED PT TO LIFEPAK 12 MONITOR. WOULD NOT GIVE ANY TYPE OF READING. ATTEMPTED TO CHANGE LEADS, CHECKED ALL CONNECTIONS, TURNED MONITOR OFF THEN BACK ON. ALL THESE MADE NO CHANGE. RED SERVICE LIGHT WAS ON AND ONLY ONE LINE ACROSS SCREEN WHEN THERE IS NORMALLY THREE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1055 MEDTRONIC PHYSIO CONTROL LIFEPAK 12 LDD MEDTRONIC PHYSIO CONTROL VLP12-02-000652 *

Patients

Seq Age Sex Outcome Treatment
1 89 YR Hospitalization| L