FDA Adverse Event Malfunction Summary report: N

CE INTERMATE LV 100, 24 PACK,50126

MDR report key: 1872968 · Received October 18, 2010

Report

Report Number
6000001-2010-04150
Event Type
Malfunction
Date Received
October 18, 2010
Date of Event
September 9, 2010
Report Date
September 16, 2010
Manufacturer
BAXTER HEALTHCARE - IRVINE
Product Code
FRN
PMA / PMN Number
K910425
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). DEVICE EVALUATION: ONE UNIT WAS RECEIVED BY BAXTER FOR EVALUATION. VISUAL EXAMINATION OF THE UNIT CONFIRMED THE DISTAL END LUER LOCK TO BE BROKEN. BAXTER HAS CONDUCTED A TREND REVIEW AND FOUND THAT SIMILAR REPORTS HAVE BEEN RECEIVED FOR THE REPORTED PROBLEM. THE ROOT CAUSE INVESTIGATION IS IN PROGRESS. A BATCH REVIEW WAS CONDUCTED AND REVEALED THAT THE PRODUCT MET ALL ACCEPTANCE CRITERIA FOR RELEASE. THIS IS A SINGLE USE DEVICE AND WILL NOT BE REPAIRED.

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 THAT THE TUBING OF ONE (1) CE INTERMATE LV100 DEVICE WAS DISCOVERED BROKEN OFF AT THE JUNCTION OF THE LUER LOCK AND BLUE WINGED CAP. THIS OCCURRED DURING FILLING WITH NORMAL SALINE. THERE HAS BEEN NO PATIENT INVOLVEMENT. NO ADDITIONAL INFORMATION IS AVAILABLE. THIS IS REPORT 2 OF 5 WITH THE SAME REPORTED PROBLEM FROM THIS FACILITY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CE INTERMATE LV 100, 24 PACK,50126 PUMP, INFUSION FRN BAXTER HEALTHCARE - IRVINE 10A002

Patients

Seq Age Sex Outcome Treatment
1