FDA Adverse Event Malfunction Summary report: N

COLLEAGUE 3CX VOLUMETRIC INFUSION PUMP

MDR report key: 1233030 · Received November 18, 2008

Report

Report Number
6000001-2007-05711
Event Type
Malfunction
Date Received
November 18, 2008
Date of Event
April 6, 2007
Report Date
April 6, 2007
Manufacturer
BAXTER HEALTHCARE PTE.LTD.
Product Code
FRN
Removal / Correction Number
2005-019-MD
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MO, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

EVALUATION SUMMARY: DURING PRODUCT EVALUATION, AIR IN LINE PRINTED CIRCUIT BOARD (AIL PCB) NEEDS CALIBRATION WAS OBSERVED. FAILURE CODE 810:04 IN THE EVENT HISTORY CONFIRMS THE AIL PCB NEEDS CALIBRATION. THIS FAILURE CODE IS MANIFESTED AS A RESULT OF THE AIL PCB BEING DEFECTIVE. THE AIL PCB ON CHANNEL A WAS RECALIBRATED.

Description of Event or Problem · 1

THE DEVICE WAS RETURNED TO BAXTER FOR SERVICE. DURING TESTING, THE BAXTER TECHNICIAN REPORTED AN INFUSION PUMP WITH A AIR IN LINE PRINTED CIRCUIT BOARD (AIL PCB) NEEDS CALIBRATION. 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 3CX VOLUMETRIC INFUSION PUMP INFUSION PUMP FRN BAXTER HEALTHCARE PTE.LTD. N/A NA

Patients

Seq Age Sex Outcome Treatment
1