FDA Adverse Event Malfunction Summary report: N

FLOGARD

MDR report key: 3183116 · Received June 21, 2013

Report

Report Number
1416980-2013-16198
Event Type
Malfunction
Date Received
June 21, 2013
Date of Event
May 21, 2013
Report Date
May 21, 2013
Manufacturer
BAXTER HEALTHCARE - SINGAPORE
Product Code
FRN
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MX
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). THE DEVICE WAS SERVICED AT THE CUSTOMER SITE AND THE SAMPLE WAS VISUALLY INSPECTED AND FUNCTIONALLY TESTED. THE REPORTED CONDITION OF CANNOT TURN ON WAS CONFIRMED AS A KEYPAD ISSUE. THE ROOT CAUSE OF THE REPORTED CONDITION WAS DUE TO A DISCONNECTED KEYPAD. TO CORRECT THE ISSUE THE KEYPAD WAS RECONNECTED. THE DEVICE WAS SERVICED AND RESTORED TO A GOOD WORKING CONDITION. IF ANY ADDITIONAL RELEVANT INFORMATION IS RECEIVED, A FOLLOW UP MDR WILL BE SENT.

Description of Event or Problem · 1

IT WAS REPORTED THAT A FLOGARD INFUSION PUMP WAS UNABLE TO TURN ON. THERE WAS NO PATIENT INVOLVEMENT. ADDITIONAL INFORMATION WAS REQUESTED AND IS NOT AVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
283969 FLOGARD PUMP, INFUSION FRN BAXTER HEALTHCARE - SINGAPORE

Patients

Seq Age Sex Outcome Treatment
1