FDA Adverse Event Malfunction Summary report: N

COLLEAGUE 3 VOLUMETRIC INFUSION PUMP

MDR report key: 1240122 · Received November 24, 2008

Report

Report Number
6000001-2007-06162
Event Type
Malfunction
Date Received
November 24, 2008
Date of Event
April 27, 2007
Report Date
April 27, 2007
Manufacturer
BAXTER HEALTHCARE PTE. LTD.
Product Code
FRN
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

EVALUATION SUMMARY: DURING PRODUCT EVALUATION, AN OUT OF SPECIFICATION AIR IN LINE PRINTED CIRCUIT BOARD (AIL PCB) WAS CONFIRMED. THE AIL PCB WAS REPLACED AND CALIBRATED.

Description of Event or Problem · 1

DURING PRODUCT EVALUATION, AN OUT OF SPECIFICATION AIR IN LINE PRINTED CIRCUIT BOARD (AIL PCB) WAS OBSERVED. THERE WAS NO PATIENT INJURY OR MEDICAL INTERVENTION NECESSARY ACCORDING TO THE HOSPITAL REPRESENTATIVE. NO ADDITIONAL INFORMATION IS AVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 COLLEAGUE 3 VOLUMETRIC INFUSION PUMP INFUSION PUMP FRN BAXTER HEALTHCARE PTE. LTD. NA NA

Patients

Seq Age Sex Outcome Treatment
1