FDA Adverse Event Malfunction Summary report: N

FLOGARD

MDR report key: 4221716 · Received November 3, 2014

Report

Report Number
1416980-2014-38588
Event Type
Malfunction
Date Received
November 3, 2014
Date of Event
October 9, 2014
Report Date
October 9, 2014
Manufacturer
BAXTER HEALTHCARE - SINGAPORE
Product Code
FRN
PMA / PMN Number
K915522
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MX
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). THE FLOGARD INFUSION PUMP WAS SERVICED ON-SITE BY A FIELD SERVICE TECHNICIAN AS PART OF PREVENTATIVE MAINTENANCE. THIS IS AN ANCILLARY SERVICE EVENT. A VISUAL INSPECTION IDENTIFIED THAT THERE WAS A DAMAGED BATTERY. THE CAUSE OF THE DAMAGE IS UNKNOWN. THE BATTERY WAS REPLACED; THE PUMP 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

DURING ON-SITE SERVICE, THE BAXTER SERVICE TECHNICIAN FOUND THAT THE FLOGARD INFUSION PUMP HAD A DAMAGED BATTERY. ADDITIONAL INFORMATION IS NOT AVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
703232 FLOGARD PUMP, INFUSION FRN BAXTER HEALTHCARE - SINGAPORE

Patients

Seq Age Sex Outcome Treatment
1