FDA Adverse Event Malfunction Summary report: N

CE INTERMATE LV 250, 24 PACK,50126

MDR report key: 2022668 · Received March 17, 2011

Report

Report Number
6000001-2011-01958
Event Type
Malfunction
Date Received
March 17, 2011
Date of Event
February 21, 2011
Report Date
March 2, 2011
Manufacturer
BAXTER HEALTHCARE - IRVINE
Product Code
FRN
PMA / PMN Number
K910425
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
WY, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). ONE SAMPLE WAS RECEIVED BY BAXTER FOR EVALUATION. THE REPORTED CONDITION OF "BROKEN JUNCTION NEAR THE LUER LOCK AND BLUE WINGED CAP" WAS CONFIRMED. THIS IS A SINGLE USE DEVICE AND WILL NOT BE REPAIRED. NO OTHER OBSERVATION WAS FOUND. SIMILAR REPORTS HAVE BEEN RECEIVED FOR THE REPORTED PROBLEM; THE ROOT CAUSE INVESTIGATION IS IN PROGRESS. A BATCH REVIEW WAS CONDUCTED AND NO ISSUES WERE FOUND RELATED TO THE REPORTED CONDITION DURING THE MANUFACTURE OF THE LOT.

Additional Manufacturer Narrative · 1

(B)(4). ADDITIONAL NARRATIVE: THE DEVICE HAS BEEN RECEIVED BY BAXTER FOR EVALUATION; HOWEVER, THE EVALUATION HAS NOT YET BEEN COMPLETED. A FOLLOW-UP REPORT WILL BE SUBMITTED UPON COMPLETION OF THE EVALUATION AND/OR SHOULD ANY ADDITIONAL INFORMATION BECOME AVAILABLE.

Description of Event or Problem · 1

IT WAS REPORTED TO BAXTER HEALTHCARE THAT ONE (1) CE INTERMATE LV250 DEVICE WAS DISCOVERED WITH BROKEN TUBING NEAR THE LUER LOCK/BLUE WINGED CAP JUNCTION. ACCORDING TO THE CUSTOMER, THIS WAS OBSERVED OUT OF THE PACKAGING/BEFORE USE. THIS DEVICE DOES HAVE THE BROKEN END PIECE TO EVALUATE. NO PATIENT INVOLVEMENT. NO ADDITIONAL INFORMATION IS AVAILABLE. THIS IS REPORT 3 OF 4 WITH THE SAME REPORTED PROBLEM FROM THIS FACILITY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CE INTERMATE LV 250, 24 PACK,50126 PUMP, INFUSION FRN BAXTER HEALTHCARE - IRVINE 10M079

Patients

Seq Age Sex Outcome Treatment
1