FDA Adverse Event Malfunction Summary report: N

CLEARLINK CONTINU-FLO 3 PORTMANIFOLD 10 DPM NV

MDR report key: 2032925 · Received March 29, 2011

Report

Report Number
6000001-2011-02328
Event Type
Malfunction
Date Received
March 29, 2011
Date of Event
October 1, 2010
Report Date
October 5, 2010
Manufacturer
BAXTER HEALTHCARE - AIBONITO
Product Code
FMG
PMA / PMN Number
K932512
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
NURSE

Narratives

Additional Manufacturer Narrative · 1

(B)(4). A 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. BAXTER HAS CONDUCTED A TREND REVIEW AND FOUND THAT SIMILAR REPORTS HAVE BEEN RECEIVED FOR THE REPORTED PROBLEM. BAXTER WILL CONTINUE TO MONITOR SAMPLE REPORTS TO DETERMINE IF FURTHER ACTIONS ARE REQUIRED. A BATCH REVIEW CANNOT BE PERFORMED SINCE THERE WAS NO LOT NUMBER PROVIDED.

Description of Event or Problem · 1

A CUSTOMER REPORTED TO BAXTER PRODUCT SURVEILLANCE OF A SEPARATION ISSUE WITH A CONTINU-FLO SOLUTION SET IN WHICH THERE WAS DIFFICULTY SECURING THE MANIFOLD PORTION OF THE TUBING WHICH CAUSED LEAKAGES IN THE OPERATING ROOM. THE CUSTOMER WAS CONNECTING THIS SET TO A MICRO CLAVE LUER. THE FACILITY IS USING A FIRM PUSH AND TWIST METHOD ALWAYS IN ORDER TO CONNECT. THIS INCIDENT OCCURRED DURING PATIENT USE. THERE WAS NO PATIENT INJURY OR MEDICAL INTERVENTION ASSOCIATED WITH THIS REPORT. NO ADDITIONAL INFORMATION WAS AVAILABLE. THIS IS REPORT 5 OF 5 OF THE SAME REPORTED PROBLEM FROM THIS FACILITY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CLEARLINK CONTINU-FLO 3 PORTMANIFOLD 10 DPM NV STOPCOCK, I.V. SET FMG BAXTER HEALTHCARE - AIBONITO

Patients

Seq Age Sex Outcome Treatment
1 MICROCLAVE LUER, UNKNOWN SOLUTION