FDA Adverse Event Malfunction Summary report: N

PATROL PUMP

MDR report key: 1061134 · Received June 13, 2008

Report

Report Number
1527460-2008-00825
Event Type
Malfunction
Date Received
June 13, 2008
Date of Event
January 1, 2008
Report Date
May 15, 2008
Manufacturer
ROSS PRODUCTS DIVISION
Product Code
LZH
PMA / PMN Number
K943733
Product Problem
Yes
Report Source
Manufacturer report
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

ABBOTT NUTRITION STANDARD PROCEDURE INCLUDES ATTEMPTING TO OBTAIN ALL REQUIRED INFORMATION FROM THE SOURCE.

Description of Event or Problem · 1

THE COMPLAINANT REPORTED AN UNDERDELIVERY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 PATROL PUMP LZH PUMP, INFUSION, ENTERAL LZH ROSS PRODUCTS DIVISION 52034

Patients

Seq Age Sex Outcome Treatment
1 86 YR