MalfunctionKRF

M SERIES

Received Dec 7, 2000

Report 1220908-2000-01320 · MDR key 308592

Device

Generic name

Defibrillator/pacemaker

Manufacturer

Zoll Medical Corp.

Model number

MSERIES

Catalog number

M SERIES

Lot number

Product problems

Device Displays Incorrect Message

Patient

Narrative

Description of Event or Problem

THE COMPLAINANT ALLEGED THAT DURING INCOMING INSPECTION OF THE DEVICE IT DISPLAYED "DEFIB FAULT 72" WHILE PERFORMING A 30 JOULE TEST DISCHARGE. THE COMPLAINANT INDICATED THERE WAS NO PT INVOLVEMENT WITH THIS REPORTED MALFUNCTION.