FDA Adverse Event Malfunction Summary report: N

PACING WIRE

MDR report key: 272443 · Received April 4, 2000

Report

Report Number
MW1018580
Event Type
Malfunction
Date Received
April 4, 2000
Manufacturer
ALTO DEVELOPMENT CORP.
Product Code
LDF
Product Problem
Yes
Report Source
Voluntary report
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

PACING WIRES FAILED TO CAPTURE. DIFFERENT WIRES WORKED FINE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 PACING WIRE PACING WIRE ADULT LDF ALTO DEVELOPMENT CORP. * 067

Patients

Seq Age Sex Outcome Treatment
1 *