FDA Adverse Event Malfunction Summary report: N

FLO-GARD 6201 VOLUMETRIC INFUSION PUMP

MDR report key: 1993590 · Received February 16, 2011

Report

Report Number
6000001-2011-01057
Event Type
Malfunction
Date Received
February 16, 2011
Date of Event
January 1, 2011
Report Date
January 26, 2011
Manufacturer
BAXTER HEALTHCARE - SINGAPORE
Product Code
FRN
PMA / PMN Number
K915522
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
PR, US
Reporter Occupation
BIOMEDICAL ENGINEER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). THE CONDITION OF OCCLUSION ALL TIME WAS NOT CONFIRMED OR DUPLICATED, THEREFORE AN ASSIGNABLE CAUSE COULD NOT BE DETERMINED. A FOLLOW-UP REPORT WILL BE SUBMITTED IF ADDITIONAL INFORMATION BECOMES AVAILABLE. (B)(4).

Additional Manufacturer Narrative · 1

BAXTER HAS CONDUCTED A TREND REVIEW AND FOUND THAT SIMILAR REPORTS HAVE BEEN RECEIVED FOR THE REPORTED PROBLEM. BAXTER WILL CONTINUE TO MONITOR SIMILAR REPORTS TO DETERMINE IF FURTHER ACTIONS ARE REQUIRED. THE DEVICE HAS NOT BEEN PREVIOUSLY SENT INTO SERVICE FOR THE REPORTED CONDITION OF OCCLUSION - FALSE. (B)(4)

Additional Manufacturer Narrative · 1

THE DEVICE HAS BEEN REQUESTED TO BE RETURNED FOR EVALUATION. UPON COMPLETION OF BAXTER'S INVESTIGATION A FOLLOW UP MEDWATCH WILL BE SUBMITTED. (B)(4).

Description of Event or Problem · 1

THE FACILITY REPRESENTATIVE REPORTED ONE FLO-GARD PUMP THAT EXPERIENCED CONSTANT FALSE OCCLUSION ALARMS. IT IS UNKNOWN WHEN THE REPORTED CONDITION OCCURRED. THE CONDITION OCCURRED IN THE PEDIATRICS UNIT. ACCORDING TO THE HOSPITAL REPRESENTATIVE, NO PATIENT INJURY OR MEDICAL INTERVENTION HAD BEEN REPORTED RELATED TO THIS DEVICE. NO ADDITIONAL INFORMATION IS AVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 FLO-GARD 6201 VOLUMETRIC INFUSION PUMP PUMP, INFUSION FRN BAXTER HEALTHCARE - SINGAPORE

Patients

Seq Age Sex Outcome Treatment
1