BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MON-A-THERM FOLEY CATHETER WITH TEMPERATURE SENSORMON-A-THERM FOLEY CATHETER

    MDR report key: 10464421 · Received August 28, 2020

    Report

    Report Number
    3005483737-2020-00015
    Event Type
    Malfunction
    Date Received
    August 28, 2020
    Date of Event
    February 8, 2018
    Report Date
    August 28, 2020
    Manufacturer
    DEGANIA MEDICAL DEVICES PVT. LTD
    Product Code
    EZL
    PMA / PMN Number
    K063442
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GM
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 1

    WE WERE UNABLE TO PERFORM DHR AS THE BATCH NUMBER IS UNKNOWN. IN PROCESS, THE ASSEMBLED CATHETERS ARE BEING TESTED 100% FOR CONDUCTIVITY AND CORRECT READING OF ROOM TEMPERATURE. EVERY BATCH IS SAMPLE TESTED FOR CORRECT TEMPERATURE READING IN CALIBRATED BATH AT 25 DEGREE AND 45 DEGREE CENTIGRADE. AS THE ACTUAL SAMPLE WAS UNAVAILABLE AND THE BATCH NUMBER IS UNKNOWN, WE WERE UNABLE TO JUSTIFY THE COMPLAINT. THIS MEDICAL DEVICE REPORT IS FILED RETROSPECTIVELY FOLLOWING FDA OBSERVATION NUMBER 4 RECEIVED BY DEGANIA MEDICAL DEVICES PVT. LTD. DURING THE FDA INSPECTION OF 4-7 OF NOVEMBER 2019. THE OBSERVATION WAS RELATED TO THE FACT THAT DEGANIA MEDICAL DEVICES PVT. LTD. DID NOT ESTABLISH PROCEDURES FOR REPORTING MDRS TO FDA AS A MANUFACTURER. TILL THEN ALL COMPLAINTS RELATED TO THE DEVICES PRODUCED BY DMD WERE ASSESSED FOR MDR REPORTABILITY AND SUBMITTED AS NECESSARY TO FDA BY DEGANIA SILICONE LTD. ANOTHER Q MEDICAL DEVICES DIVISION CLOSELY AFFILIATED WITH DMD. DMD CAPA NUMBER (B)(4) WAS ISSUED TO ADDRESS THE OBSERVATION; ONE OF THE CAPA ACTIONS REQUIRES DMD TO PERFORM RETROSPECTIVE REVIEW OF ALL THE COMPLAINTS RECEIVED DURING 2018 AND 2019 AND SUBMIT TO FDA RETROSPECTIVE MDRS FOR THE REPORTABLE EVENTS (WITH REFERENCE TO ORIGINAL MDR REPORT #8030107-2020-00022 FILED BY DEGANIA SILICONE LTD.).

    Description of Event or Problem · 1

    THIS IS RETROSPECTIVE SUBMISSION, FOLLOWING REASSESSMENT OF OUR CUSTOMER COMPLAINTS DURING PERIOD 2018-2019. CUSTOMER'S TEXT: ACCORDING TO THE REPORTER, POSTOPERATIVELY, AN ISSUE WITH THE TEMPERATURE CABLES WAS OBSERVED. IT WAS REPORTED THAT THE CATHETER (37.5 DEGREES) GAVE THE WRONG TEMPERATURE AFTER CONTROL WITH THE EAR TEMPERATURE (38.7 DEGREES). THE CUSTOMER INDICATED THAT THERE WERE NO PATIENT SYMPTOMS OR COMPLICATIONS OR HARM ASSOCIATED WITH THIS EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    929044 MON-A-THERM FOLEY CATHETER WITH TEMPERATURE SENSORMON-A-THERM FOLEY CATHETER TEMPERATURE SENSING 100% SILICONE FOLEY CATHETER EZL DEGANIA MEDICAL DEVICES PVT. LTD 14 FRENCH

    Patients

    Seq Age Sex Outcome Treatment
    1