FDA Adverse Event Malfunction Summary report: N

COLLEAGUE CX TRIPLE CHANNEL VOLUMETRIC INFUSION PUMP

MDR report key: 1913630 · Received December 3, 2010

Report

Report Number
6000001-2010-05429
Event Type
Malfunction
Date Received
December 3, 2010
Date of Event
November 8, 2010
Report Date
November 8, 2010
Manufacturer
BAXTER HEALTHCARE - SINGAPORE
Product Code
FRN
PMA / PMN Number
K041191
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IL, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). A TREND REVIEW HAS BEEN PERFORMED AND THERE HAVE BEEN SIMILAR REPORTS MADE TO BAXTER. BAXTER WILL CONTINUE TO MONITOR SIMILAR REPORTS FOR TRACKING AND TRENDING PURPOSES.

Additional Manufacturer Narrative · 1

(B)(4).A FOLLOW-UP MEDWATCH REPORT WILL BE SUBMITTED WHEN THE EVALUATION RESULTS OR IF ADDITIONAL INFORMATION BECOMES AVAILABLE.

Additional Manufacturer Narrative · 1

(B)(4). DEVICE EVALUATION: THE REPORTED CONDITION WAS CONFIRMED BUT NOT DUPLICATED. THE ASSIGNABLE CAUSE WAS A FAULTY PHM (PUMPHEAD MODULE). THE PHM HAS BEEN REPLACED. ADDITIONAL: THE SERVICE HISTORY REVIEW REVEALED THAT THIS DEVICE WAS NOT PREVIOUSLY SERVICED FOR THE REPORTED CONDITION.

Description of Event or Problem · 1

DURING THE PRODUCT EVALUATION AT BAXTER, IT WAS DISCOVERED THAT THE COLLEAGUE INFUSION PUMP HAD AN UPSTREAM OCCLUSION ON CHANNEL C. THERE WAS AN UPSTREAM OCCLUSION FALSE ALARM THAT OCCURRED. THERE WAS NO ADVERSE EVENT, PATIENT INJURY OR MEDICAL INTERVENTION ASSOCIATED WITH THIS REPORT. THERE IS NO FURTHER COMPLAINT INFORMATION AVAILABLE. THE USER INTERFACE MODULE MASTER SOFTWARE VERSION IS CURRENTLY UNKNOWN FOR THIS DEVICE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 COLLEAGUE CX TRIPLE CHANNEL VOLUMETRIC INFUSION PUMP PUMP, INFUSION FRN BAXTER HEALTHCARE - SINGAPORE

Patients

Seq Age Sex Outcome Treatment
1