FDA Adverse Event Malfunction Summary report: N

DIALYZER, HIGH PERMEABILITY WITH OR WITHOUT SEALED DIALYSATE SYSTEM

MDR report key: 3024215 · Received March 27, 2013

Report

Report Number
1416980-2013-07516
Event Type
Malfunction
Date Received
March 27, 2013
Date of Event
February 19, 2013
Report Date
March 6, 2013
Manufacturer
BAXTER HEALTHCARE - SWINFORD
Product Code
KDI
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

(B)(4). THE SAMPLE HAS BEEN REPORTED TO BE AVAILABLE FOR EVALUATION AND HAS BEEN REQUESTED; HOWEVER, THE SAMPLE HAS NOT BEEN RECEIVED FOR EVALUATION. A FOLLOW-UP REPORT WILL BE FILED IF ADDITIONAL INFORMATION IS RECEIVED.

Additional Manufacturer Narrative · 1

(B)(4). THIS COMPLAINT WAS CONFIRMED DURING EVALUATION OF THE RETURNED SAMPLE; HOWEVER, NO ROOT CAUSE COULD BE DETERMINED. A VISUAL INSPECTION WAS PERFORMED THERE WERE CRACKS ON THE MINICAP NOTED. FUNCTIONAL TESTING WAS PERFORMED AND ALL CRITICAL DIMENSIONS WERE MEASURED AND WERE FOUND TO BE WITHIN THE SPECIFIED TOLERANCES PER THE RELEVANT MINICAP DRAWING. THE MANUFACTURING BATCH RECORD REVIEW CONFIRMED THAT THE DEVICE MET ALL MATERIAL, ASSEMBLY AND PERFORMANCE SPECIFICATIONS. IF ADDITIONAL RELEVANT INFORMATION IS RECEIVED A FOLLOW-UP WILL BE SUBMITTED.

Description of Event or Problem · 1

IT WAS REPORTED THAT A PATIENT HAD A LEAK DURING PERITONEAL DIALYSIS (PD) THERAPY. IT WAS REPORTED THAT A POVIDONE IODINE LEAK FROM A CRACK ON THE MINICAP WAS FOUND DURING USE. THERE WAS PATIENT INVOLVEMENT, BUT THERE WAS NO PATIENT INJURY OR MEDICAL INTERVENTION INDICATED AT THE TIME OF THE INITIAL REPORT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
125949 DIALYZER, HIGH PERMEABILITY WITH OR WITHOUT SEALED DIALYSATE SYSTEM KDI BAXTER HEALTHCARE - SWINFORD 12H29H17

Patients

Seq Age Sex Outcome Treatment
1