FDA Adverse Event Malfunction Summary report: N

COLLEAGUE CX VOLUMETRIC INFUSION PUMP

MDR report key: 1233083 · Received November 18, 2008

Report

Report Number
6000001-2007-05962
Event Type
Malfunction
Date Received
November 18, 2008
Date of Event
April 1, 2007
Report Date
April 3, 2007
Manufacturer
BAXTER HEALTHCARE PTE. LTD.
Product Code
FRN
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
GA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE FACILITY REPORTED AN INFUSION PUMP WITH A FAILURE CODE 814:04 CONDITION. EVALUATION SUMMARY: DURING PRODUCT EVALUATION, A DEFECTIVE AIL (AIR IN LINE) PCB (PRINTED CIRCUIT BOARD) WAS OBSERVED. FAILURE CODE 814:04 IN THE EVENT HISTORY CONFIRMS THE DEFECTIVE AIL PCB. THIS FAILURE CODE IS MANIFESTED AS A RESULT OF THE AIL PCB BEING DEFECTIVE. THE AIL PCB WAS REPLACED. REVIEW OF THE COMPLAINT HISTORY REVEALS SIMILAR REPORTS HAVE BEEN RECEIVED FOR THIS PRODUCT FOR THE REPORTED ISSUE. THIS ISSUE IS BEING INVESTIGATED.

Description of Event or Problem · 1

THE DEVICE WAS RETURNED TO BAXTER FOR SERVICE. DURING TESTING, THE BAXTER TECHNICIAN REPORTED AN INFUSION PUMP WITH AN AIL (AIR IN LINE) PCB (PRINTED CIRCUIT BOARD) MALFUNCTION. ACCORDING TO THE HOSPITAL REPRESENTATIVE, NO PATIENT INJURY OR MEDICAL INTERVENTION HAS BEEN REPORTED RELATED TO THIS DEVICE. NO ADDITIONAL INFORMATION IS KNOWN.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1