FDA Adverse Event Malfunction Summary report: N

PUMP,COLLEAGUE CXE SINGLECHANNEL COLOUR FRENCH LOANER

MDR report key: 1981125 · Received February 8, 2011

Report

Report Number
6000001-2011-00729
Event Type
Malfunction
Date Received
February 8, 2011
Date of Event
December 16, 2010
Report Date
December 22, 2010
Manufacturer
BAXTER HEALTHCARE - SINGAPORE
Product Code
FRN
Removal / Correction Number
6000001-12/1/-08-002-C
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA
Reporter Occupation
BIOMEDICAL ENGINEER

Narratives

Additional Manufacturer Narrative · 1

THE CONDITION OF DEPLETED BATTERY ALARM WAS CONFIRMED THROUGH THE EVENT HISTORY. THE CONDITION IS DUE TO DEPLETED MAIN BATTERIES. THE MAIN BATTERIES WERE REPLACED. SHOULD ADDITIONAL INFORMATION BECOME AVAILABLE A FOLLOW UP MEDWATCH WILL BE SUBMITTED. THIS PRODUCT IS MANUFACTURED FOR DISTRIBUTION OUTSIDE OF THE UNITED STATES (US); THEREFORE, IT DOES NOT HAVE A US 510K NUMBER. HOWEVER, THIS MDR IS BEING SUBMITTED BECAUSE IT IS THE SAME AS OR SIMILAR TO A PRODUCT DISTRIBUTED WITHIN THE US. (B)(4).

Additional Manufacturer Narrative · 1

(B)(4). SIMILAR REPORTS HAVE BEEN RECEIVED FOR THE REPORTED PROBLEM. THE ROOT CAUSE INVESTIGATION IS IN PROGRESS THROUGH CAPA (B)(4).

Description of Event or Problem · 1

THIS IS A REPORT FROM BAXTER (B)(4) OF A BATTERY ISSUE. IT IS UNKNOWN WHEN THE REPORTED CONDITION OCCURRED. NO PATIENT INJURY OR MEDICAL INTERVENTION OCCURRED. DURING A REVIEW OF THE PUMP'S EVENT HISTORY BY BAXTER (B)(4) PERSONNEL, A COLLEAGUE INFUSION PUMP WAS FOUND TO HAVE EXPERIENCED A DEPLETED BATTERY ALARM WHICH INTERRUPTED DELIVERY. NO ADDITIONAL INFORMATION IS AVAILABLE. THIS DEVICE UTILIZES USER INTERFACE MODULE MASTER SOFTWARE VERSION 6.63.92 CATEGORIZED AS REMEDIATED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 PUMP,COLLEAGUE CXE SINGLECHANNEL COLOUR FRENCH LOANER PUMP, INFUSION FRN BAXTER HEALTHCARE - SINGAPORE

Patients

Seq Age Sex Outcome Treatment
1