FDA Adverse Event Malfunction Summary report: N

CONTINU-FLO SOL SET 10 DPM 106W/ 1CL Y & .22 MICRON FILTER

MDR report key: 1940010 · Received December 28, 2010

Report

Report Number
6000001-2010-06281
Event Type
Malfunction
Date Received
December 28, 2010
Date of Event
December 1, 2010
Report Date
December 3, 2010
Manufacturer
BAXTER HEALTHCARE
Product Code
FPA
PMA / PMN Number
K964850
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

(B)(4). IT IS UNKNOWN IF A SAMPLE IS AVAILABLE FOR EVALUATION. IF ADDITIONAL INFORMATION OR SAMPLES BECOME AVAILABLE, A FOLLOW UP REPORT WILL BE SUBMITTED.

Additional Manufacturer Narrative · 1

(B)(4). THE SAMPLE IS NOT AVAILABLE FOR EVALUATION, THEREFORE, THE CONDITION CANNOT BE CONFIRMED OR DUPLICATED AND THE ASSIGNABLE ROOT CAUSE COULD NOT BE DETERMINED. IF ADDITIONAL INFORMATION OR SAMPLES BECOME AVAILABLE, A FOLLOW UP REPORT WILL BE SUBMITTED. A BATCH REVIEW COULD NOT BE PERFORMED AS THE LOT NUMBER IS UNKNOWN. 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.

Description of Event or Problem · 1

THE FACILITY REPRESENTATIVE REPORTED TO BAXTER AN UNKNOWN NUMBER OF FLO GARD INFUSION PUMPS WHICH WERE INVOLVED IN AN INCIDENT WHERE OCCLUSIONS WERE CAUSED BY THE CONTINU-FLO SOLUTION SET WITH 0.22 MICRON FILTER WHILE BEING USED WITH CLEAR TPN. IT IS UNKNOWN WHEN THIS EVENT OCCURRED. NO PATIENT INJURY OR MEDICAL INTERVENTION WAS REPORTED. NO ADDITIONAL INFORMATION IS AVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CONTINU-FLO SOL SET 10 DPM 106W/ 1CL Y & .22 MICRON FILTER SET, ADMINISTRATION, INTRAVASCULAR FPA BAXTER HEALTHCARE

Patients

Seq Age Sex Outcome Treatment
1 CLEAR TOTAL PARENTERAL NUTRITION| FLOGARD PUMP