FDA Adverse Event Malfunction Summary report: N

PATROL PUMP

MDR report key: 2040283 · Received February 15, 2011

Report

Report Number
1527460-2011-00014
Event Type
Malfunction
Date Received
February 15, 2011
Report Date
February 14, 2011
Manufacturer
ABBOTT NUTRITION
Product Code
LZH
PMA / PMN Number
K943733
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

(B)(4): THE TESTING AND INVESTIGATION RESULTS CONFIRMED AN UNDER-DELIVERY WITH A STUTTERING MOTOR. THE POLE PIECES OF THE MOTOR WERE FOUND TO BE MISALIGNED. ABBOTT NUTRITION STANDARD PROCEDURE INCLUDES ATTEMPTING TO OBTAIN ALL REQUIRED INFO FROM THE SOURCE.

Description of Event or Problem · 1

THE DEVICE EVAL IDENTIFIED A REPORTABLE MALFUNCTION, UNDER-DELIVERY, RELATED TO THE ORIGINAL COMPLAINT, WHICH WAS NOT A REPORTABLE EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 PATROL PUMP LZH, PUMP, INFUSION, ENTERAL LZH ABBOTT NUTRITION 52036

Patients

Seq Age Sex Outcome Treatment
1