FDA Adverse Event Malfunction Summary report: N

INTERMATE

MDR report key: 3941177 · Received July 17, 2014

Report

Report Number
1416980-2014-22984
Event Type
Malfunction
Date Received
July 17, 2014
Date of Event
June 24, 2014
Report Date
June 24, 2014
Manufacturer
BAXTER HEALTHCARE - IRVINE
Product Code
FRN
PMA / PMN Number
K910425
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
UK
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). IF ADDITIONAL RELEVANT INFORMATION IS OBTAINED, THEN A FOLLOW-UP MDR WILL BE SUBMITTED.

Additional Manufacturer Narrative · 1

(B)(4). A CAPA HAS BEEN OPENED FOR THIS ISSUE. SHOULD ADDITIONAL RELEVANT INFORMATION BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED.

Additional Manufacturer Narrative · 1

(B)(4). THE LOT WAS MANUFACTURED FROM MARCH 18, 2013 TO MARCH 19, 2013. EVALUATION SUMMARY: THE DEVICE WAS RETURNED FOR EVALUATION. VISUAL INSPECTION, VIA THE NAKED EYE, NOTED SOLID WHITE PARTICLES, BETWEEN 0.15 AND 0.70 MM IN SIZE, FLOATING IN THE FLUID OF THE BLADDER. FOURIER TRANSFORM INFRARED (FT-IR) SPECTROSCOPY SCANNING IDENTIFIED THE PARTICLES TO BE ACRYLIC MATERIAL. A REVIEW OF ALL BATCH RECORD DOCUMENTS WAS PERFORMED WITH NO ISSUES NOTED DURING THE MANUFACTURING PROCESS. THERE WERE NO DEVIATIONS FROM STANDARD PROCEDURE AND NO EXCEPTIONS RELATED TO THE REPORTED CONDITION WERE NOTED. THE CAUSE OR ORIGIN OF THE PARTICLES WAS UNABLE TO BE DETERMINED. SHOULD ADDITIONAL RELEVANT INFORMATION BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED.

Description of Event or Problem · 1

IT WAS REPORTED THAT AN INTERMATE HAD PARTICULATE MATTER INSIDE ITS BALLOON. THERE WAS NO PATIENT INVOLVEMENT. ADDITIONAL INFORMATION WAS REQUESTED AND IS NOT AVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
419710 INTERMATE PUMP, INFUSION FRN BAXTER HEALTHCARE - IRVINE 14C045

Patients

Seq Age Sex Outcome Treatment
1