FDA Adverse Event Malfunction Summary report: N

AUTOPULSE NIMH BATTERY

MDR report key: 2935766 · Received January 2, 2013

Report

Report Number
3003793491-2012-00694
Event Type
Malfunction
Date Received
January 2, 2013
Date of Event
November 12, 2012
Report Date
November 12, 2012
Manufacturer
ZOLL CIRCULATION, INC.
Product Code
DRM
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MA, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

THE AUTOPULSE NIMH BATTERY (S/N (B)(4)) INVOLVED IN THE EVENT WAS RETURNED TO ZOLL MEDICAL CORPORATION ON (B)(4) 2012 AND WAS ANALYZED. VISUAL INSPECTION OF THE BATTERY SHOWED NO DAMAGES. REPORTED PROBLEM WAS CONFIRMED. THE BATTERY FAILED TESTING AND WILL BE SCRAPPED. PROBABLE CAUSE FOR BATTERY FAILING COULD BE DUE TO AGING (MANUFACTURED IN AUGUST 2010) OR IMPROPER BATTERY MAINTENANCE. THE CALENDAR AGE OF THE BATTERY IS GREATER THAN 2 YEARS. THE PRODUCT LABELING INSTRUCTS THAT THE USEFUL LIFE OF EACH AUTOPULSE BATTERY IS BETWEEN 2-4 YEARS. AS WITH ALL BATTERIES, THE NIMH BATTERY CHEMISTRY HAS A FINITE CALENDER LIFE. WITHIN THE 2-4 YEAR LIFE RANGE, THE LIFE OF EACH BATTERY IS INFLUENCED BY THE FREQUENCY OF USE AND THE FREQUENCY OF ROUTINE BATTERY MAINTENANCE. BATTERY SERIAL NUMBER (B)(4) WAS RECEIVED AND SERVICED ON (B)(4) 2012. THE AUTOPULSE SYSTEM LABELING REQUIRES THE USER TO "TEST CYCLE" EACH BATTERY MONTHLY. THE NUMBER OF TEST CYCLES OBTAINED FOR THIS BATTERY WAS "13" CYCLES. IF PROPER BATTERY MANAGEMENT HAD BEEN FOLLOWED, THE EXPECTED NUMBER OF TEST CYCLES WOULD BE "27". NOT FOLLOWING THE RECOMMENDED BATTERY MAINTENANCE MAY RESULT IN FASTER AGING. THIS LACK OF TEST CYCLES MAY HAVE CONTRIBUTED TO THE BATTERY END OF LIFE. NO ADVERSE EVENT WAS REPORTED.

Description of Event or Problem · 1

IT WAS REPORTED THAT BATTERY HAS LOW POWER.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1589 AUTOPULSE NIMH BATTERY NIMH BATTERY DRM ZOLL CIRCULATION, INC.

Patients

Seq Age Sex Outcome Treatment
1 Other