FDA Adverse Event Malfunction Summary report: N

COLLEAGUE SINGLE CHANNEL VOLUMETRIC PUMP CE FRENCH

MDR report key: 1843073 · Received September 23, 2010

Report

Report Number
6000001-2010-03501
Event Type
Malfunction
Date Received
September 23, 2010
Date of Event
July 28, 2010
Report Date
July 29, 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
OTHER

Narratives

Additional Manufacturer Narrative · 1

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. THE CONDITION OF BATTERY ISSUE WAS CONFIRMED THROUGH AN ONSITE REPAIR. THE CONDITION IS DUE TO DEPLETED MAIN BATTERIES. THE MAIN BATTERIES WERE REPLACED. (B)(4)

Additional Manufacturer Narrative · 1

BAXTER HAS CONDUCTED A TREND REVIEW AND FOUND THAT SIMILAR REPORTS HAVE BEEN RECEIVED FOR THE REPORTED PROBLEM. THE ROOT CAUSE INVESTIGATION IS IN PROGRESS THROUGH (B)(4). THE DEVICE HAS PREVIOUSLY BEEN SERVICED BY BAXTER. THE BATTERY HAS PREVIOUSLY BEEN REPLACED. (B)(4).

Description of Event or Problem · 1

DURING A REVIEW OF THE PUMP'S EVENT HISTORY BY BAXTER (B)(4) PERSONNEL, A COLLEAGUE INFUSION PUMP WAS FOUND TO HAVE EXPERIENCED A BATTERY DEPLETED ALARM WHICH INTERRUPTED DELIVERY. THERE WAS NO REPORT OF PATIENT INJURY, MEDICAL INTERVENTION NECESSARY OR ADVERSE REACTION IN ASSOCIATION WITH THIS EVENT. NO ADDITIONAL INFORMATION IS AVAILABLE. THIS DEVICE UTILIZES USER INTERFACE MODULE MASTER SOFTWARE VERSION 5.08.92 CATEGORIZED AS REMEDIATED.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1