FDA Adverse Event Malfunction Summary report: N

COLLEAGUE VOLUMETRIC INFUSION PUMP

MDR report key: 1023180 · Received April 4, 2008

Report

Report Number
6000001-2007-00741
Event Type
Malfunction
Date Received
April 4, 2008
Date of Event
December 1, 2006
Report Date
December 11, 2006
Manufacturer
BAXTER HEALTHCARE PTE. LTD.
Product Code
FRN
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IL, US
Reporter Occupation
BIOMEDICAL ENGINEER

Narratives

Additional Manufacturer Narrative · 1

EVALUATION SUMMARY:THE DEVICE EVALUATION WAS COMPLETED AND FAILURE CODE 500:320:675:0000 CONFIRMED (IN EVENT HISTORY) DUE TO A STUCK KEY ON THE FRONT BEZEL KEYPAD. SERVICE INSTALLED A NEW FRONT BEZEL AND TESTED THE DEVICE. A REVIEW OF THE COMPLAINT HISTORY REVEALED SIMILAR REPORTS HAVE BEEN RECEIVED FOR THIS PRODUCT AND THE REPORTED ISSUE. THIS ISSUE IS BEING INVESTIGATED UNDER CAPA.

Description of Event or Problem · 1

THE FACILITY REPRESENTATIVE REPORTED, A PUMP WITH AN INTERMITTENT 500:320:675:0000 FAILURE CODE. THE CONDITION WAS DISCOVERED DURING BIO-MED TESTING. ACCORDING TO THE HOSPITAL REPRESENTATIVE, THERE WAS NO PATIENT INJURY OR MEDICAL INTERVENTION REPORTED. NO ADDITIONAL INFORMATION WAS PROVIDED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 COLLEAGUE VOLUMETRIC INFUSION PUMP INFUSION PUMP FRN BAXTER HEALTHCARE PTE. LTD. NA NA

Patients

Seq Age Sex Outcome Treatment
1