FDA Adverse Event Malfunction Summary report: N

FLOGARD

MDR report key: 2173571 · Received July 23, 2011

Report

Report Number
6000001-2011-13609
Event Type
Malfunction
Date Received
July 23, 2011
Date of Event
May 31, 2011
Report Date
June 1, 2011
Manufacturer
BAXTER HEALTHCARE - SINGAPORE
Product Code
FRN
PMA / PMN Number
K915522
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
PR
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). THE DEVICE WAS RETURNED TO BAXTER AND IS CURRENTLY AWAITING EVALUATION. A FOLLOW-UP REPORT WILL BE FILED UPON COMPLETION OF THE EVALUATION OR IF ANY ADDITIONAL DETAILS BECOME AVAILABLE.

Additional Manufacturer Narrative · 1

(B)(4). THE CONDITION FOR THE FLO-GARD INFUSION PUMP WAS NOT CONFIRMED AND NOT DUPLICATED DURING PRODUCT EVALUATION. THEREFORE, NO ASSIGNABLE CAUSE COULD BE PROVIDED FOR THIS CONDITION AND NO REPAIR WAS NECESSARY. A SERVICE HISTORY REVIEW REVEALED NO PREVIOUS SERVICE EVENTS WERE RELATED TO THE REPORTED CONDITION. THE DEVICE HISTORY RECORD REVIEW REVEALVED THAT THE DATA CARD WAS DISCARDED PER (B)(4) RETENTION PERIOD.

Description of Event or Problem · 1

THE FACILITY REPORTED A FLO-GARD INFUSION PUMP WITH A MALFUNCTION OF "DAMAGE, INFUSION NOT LOWER." AFTER FURTHER INVESTIGATION, THE FACILITY LATER CLARIFIED THAT THE MALFUNCTION OF THE DEVICE WAS THAT THE " EQUIPMENT WILL NOT DISPENSE." THE EVENT WAS REPORTED TO HAVE OCCURRED UPON POWER UP IN THE INTENSIVE CARE UNIT. THE HOSPITAL REPRESENTATIVE DID NOT HAVE ANY INFORMATION ON PATIENT INVOLVEMENT. NO PATIENT INJURY OR MEDICAL INTERVENTION HAD BEEN REPORTED RELATED TO THE DEVICE. NO ADDITIONAL INFORMATION IS AVAILABLE.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1