BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    DUODERM PASTE AND GELS

    MDR report key: 15742253 · Received November 7, 2022

    Report

    Report Number
    1000317571-2022-00334
    Event Type
    Malfunction
    Date Received
    November 7, 2022
    Report Date
    October 13, 2022
    Manufacturer
    CONVATEC DOMINICAN REPUBLIC INC
    Product Code
    NAE
    UDI-DI
    00768455172979
    PMA / PMN Number
    EXEMPT
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    003

    Narratives

    Additional Manufacturer Narrative · 0

    INITIAL REPORTER NAME AND ADDRESS: COMPLAINANT CITY: LIMA. COMPLAINANT STATE: LIMA. COMPLAINANT COUNTRY: PERU. NAME OF AFFILIATION: CARDIO PERFUSION E.I.R.L. BASED ON THE AVAILABLE INFORMATION, THIS EVENT IS DEEMED TO BE A REPORTABLE MALFUNCTION. TO DATE NO ADDITIONAL INFORMATION HAS BEEN RECEIVED. SHOULD ADDITIONAL INFORMATION BECOME AVAILABLE, A FOLLOW-UP REPORT WILL BE SUBMITTED. (B)(4).

    Additional Manufacturer Narrative · 0

    ADDITIONAL INFORMATION - THIS EMDR IS BEING SUBMITTED TO INCLUDE THE BELOW: H6 - INVESTIGATION RESULTS UNDER IMDRF CAUSE INVESTIGATION CODE, IMDRF INVESTIGATION FINDINGS, IMDRF CAUSE CONCLUSIONS. H6: IMDRF INVESTIGATION FINDINGS HAS BEEN SELECTED AS C22 FOR TERM "IMPROPER PRINTING WHILE LABELLING PROCESS". BATCH RECORD REVIEW: A BATCH RECORD REVIEW WAS COMPLETED AND NO DISCREPANCIES WERE FOUND. DUODERM H/ACTIVE GEL (3TBEX30G) STER US WAS MANUFACTURED UNDER SYSTEM APPLICATION PRODUCT (SAP) CODE 1002859 AND MANUFACTURING LOT NUMBER 2A02569 ON 08 FEB 2022. LOT # 2A02569 WAS STERILISED UNDER REFERENCE 22A10K7775 AND 22A10K7773 AND RELEASED ON REVIEW OF RESULTS OF STERILISATION PROVIDED BY STERILISATION COMPANY BAXTER. ALL OF THE RESULTS WERE WITHIN SPECIFICATION AND PRODUCTS WERE RELEASED. NO NONCONFORMITY WAS IDENTIFIED DURING THE MANUFACTURING PROCESS OF LOT 2A02569, BUT A NONCONFORMITY WAS RAISED FOLLOWING STERILISATION FOR AN UNRELATED MATTER. THERE ARE 2 COMPLAINTS AGAINST LOT 2A02568, INCLUDING THIS COMPLAINT. THE ADDITIONAL COMPLAINT IS RELATED TO THIS COMPLAINT AND COVERS THE DAMAGE ASPECT OF THE COMPLAINT RECEIVED. ONE PHOTOGRAPH WAS RECEIVED FOR THIS ISSUE AND HAVE BEEN EVALUATED IN ACCORDANCE WITH WORK INSTRUCTION (WI). THE PHOTOGRAPHS CONFIRM THE EXPECTED LOT NUMBER, PRODUCT AND THE COMPLAINT ISSUE. THE IMAGE SHOWS 6 TUBES WITH RED RINGS MARKING THE STAINING, WHERE A SINGLE ROUND-SHAPED IMPERFECTION OR CHIP IN THE PAINT MAY BE SEEN, AND ALSO A BLACK DOT. THE OTHER RED RINGS APPEAR TO BE MARKING TUBE DAMAGE. IT WAS NOT POSSIBLE TO HAVE THE SAMPLE RETURNED DUE TO COURIER RESTRICTIONS IN THE LATAM (LATIN AMERICA) REGION FOR THE PRODUCT, SO IT WAS NOT POSSIBLE TO IDENTIFY WHAT THE ¿STAINING¿ COULD BE. A PREVIOUS NONCONFORMANCE WAS OPENED FOR THIS COMPLAINT BATCH. TRIAGE IDENTIFIED THAT THE PHOTOGRAPHS RECEIVED SHOWED THE TUBE TO HAVE PRINTED INFORMATION NOT APPLIED AT THE MANUFACTURING SITE. LATAM REGULATORY REPRESENTATIVES CONFIRMED THIS RELABELLING ACTIVITY IS COMPLETED IN CARIBETRANS LATAM WAREHOUSES DUE TO LOCAL REQUIREMENTS USING AN INKJET PRINTER. THE OFFSET IN THE PRINTING IN THIS COMPLAINT WILL BE A PRINT DEFECT FROM THE CARIBETRANS RELABELLING PROCESS FOR THE LATAM REGION. THE SUPPLIER HAS BEEN MADE AWARE. THE DEFECTS CIRCLED RED ON THE PHOTOGRAPH APPEARED TO BE A SLIGHT INDENT, NOT ALLOWABLE BY THE STANDARDS OF ACCEPTABILITY, BUT IT IS NOT CLEAR IF THIS IS A DEFECT FROM THE SUPPLIER, DAMAGE SUSTAINED DURING TRANSIT OR DAMAGE SUSTAINED DURING THE RELABELLING PROCESS FOR THE LATAM REGION. THIS CAN ALSO BE SAID ABOUT THE BLACK DOT. IT IS NOT CLEAR WHERE THIS HAS COME FROM, POSSIBLY FROM THE RELABELLING PROCESS OR IT WAS PRESENT ON THE TUBE UPON RECEIPT FROM THE SUPPLIER. IT DOES NOT OBSCURE ANY LABELLING THIS ISSUE WILL BE MONITORED THROUGH THE POST MARKET PRODUCT MONITORING REVIEW PROCESS. TO DATE NO ADDITIONAL INFORMATION HAS BEEN RECEIVED. SHOULD ADDITIONAL INFORMATION BECOME AVAILABLE, A FOLLOW-UP REPORT WILL BE SUBMITTED. FDA REGISTRATION NUMBER: REPORTING SITE: 1049092. MANUFACTURING SITE: 1000317571.

    Description of Event or Problem · 0

    IT WAS REPORTED THAT THE GEL TUBE HAD STAINED AND BUMPED ON THE ALUMINUM TUBE AND SEVEN UNITS WERE AFFECTED. THE PRODUCT WAS NOT USED ON PATIENT. A PHOTOGRAPH DEPICTING THE ISSUE WAS RECEIVED FROM THE COMPLAINANT.

    Description of Event or Problem · 0

    TO DATE NO ADDITIONAL PATIENT OR EVENT DETAILS HAVE BEEN RECEIVED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    212274 DUODERM PASTE AND GELS NOT APPLICABLE NAE CONVATEC DOMINICAN REPUBLIC INC 187987 2A02569 00768455172979

    Patients

    Seq Age Sex Outcome Treatment
    1 Unknown