FDA Adverse Event Malfunction Summary report: N

PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

MDR report key: 3151867 · Received June 7, 2013

Report

Report Number
2183613-2013-00556
Event Type
Malfunction
Date Received
June 7, 2013
Date of Event
March 18, 2013
Report Date
March 18, 2013
Manufacturer
MEDTRONIC MILACA, INC.
Product Code
LWP
PMA / PMN Number
P820003
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
AS
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THIS EVENT OCCURRED OUTSIDE THE US WHERE THE SAME MODEL IS DISTRIBUTED. ALL INFORMATION PROVIDED IS INCLUDED IN THIS REPORT. PATIENT INFORMATION IS NOT GENERALLY AVAILABLE DUE TO CONFIDENTIALITY CONCERNS. (B)(4).

Additional Manufacturer Narrative · 1

PRODUCT EVENT SUMMARY: THE GENERATOR WAS RETURNED AND ANALYSIS COULD NOT CONFIRM THE CUSTOMER COMMENT THAT THERE WAS NO BATTERY BACK UP WHEN THE OLD BATTERY WAS CHANGED OUT. ANALYSIS DID FIND THE UPPER CASE, RING COVER AND ONE HEART WIRE CONTACT CONTAMINATED, THE LOWER CASE AND BATTERY DRAWER BROKEN, THE BATTERY CONTACTS COMPRESSED AND THE KEYBOARD SCRATCHED.

Additional Manufacturer Narrative · 1

IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE EXTERNAL PULSE GENERATOR HAD NO BATTERY BACK UP WHEN CHANGING OUT AN OLD BATTERY FOR A NEW ONE. THE GENERATOR WAS RETURNED FOR SERVICE. NO PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE EXTERNAL PULSE GENERATOR HAD NO BATTERY BACK UP WHEN CHANGING OUT AN OLD BATTERY FOR A NEW ONE. THE GENERATOR WAS RETURNED FOR SERVICE. NO PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
253260 PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE LWP MEDTRONIC MILACA, INC. 5388X

Patients

Seq Age Sex Outcome Treatment
1