BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PVA FOAM EMBOLIZATION PARTICLES

    MDR report key: 7372437 · Received March 26, 2018

    Report

    Report Number
    1820334-2018-00675
    Event Type
    Malfunction
    Date Received
    March 26, 2018
    Date of Event
    March 5, 2018
    Report Date
    May 22, 2018
    Manufacturer
    COOK INC
    Product Code
    KRD
    UDI-DI
    00827002096653
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CN
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    COMMON DEVICE NAME: AGENTS, EMBOLIC, FOR TREATMENT OF UTERINE FIBROIDS; PROCODE: NAJ. (B)(4). PMA/510K #: K081768. THIS REPORT INCLUDES INFORMATION KNOWN AT THIS TIME. A FOLLOW UP REPORT WILL BE SUBMITTED SHOULD ADDITIONAL RELEVANT INFORMATION BECOME AVAILABLE.

    Additional Manufacturer Narrative · 1

    INVESTIGATION ¿ EVALUATION: A REVIEW OF THE COMPLAINT HISTORY, DEVICE HISTORY RECORD, DOCUMENTATION, INSTRUCTIONS FOR USE (IFU), MANUFACTURING INSTRUCTIONS, QUALITY CONTROL, AND SPECIFICATIONS OF THE DEVICE WAS CONDUCTED DURING THE INVESTIGATION. VIAL OF PVA RETURNED IN A USED CONDITION. THE VIAL APPEARED TO HAVE BIOMATTER ON THE OUTSIDE AND WAS STICKY TO THE TOUCH. THE VIAL WAS NEARLY EMPTY. THE MAJORITY OF THE PARTICLES ARE WHITE AND CONSISTENT WITH PVA. THERE ARE SEVERAL BROWN PARTICLES ADHERING TO THE SIDES OF THE INSIDE OF THE VIAL, WHILE THE WHITE PARTICLES MOVE FREELY. THE REDDISH-BROWN PARTICLES ARE THE SAME SIZE AS THE WHITE PARTICLES. IT APPEARS THAT A FOREIGN SUBSTANCE MAY HAVE SPILLED INTO THE PVA, CAUSING SOME OF THE PARTICLES TO BE CONTAMINATED.¿ ADDITIONALLY, A DOCUMENT BASE INVESTIGATION EVALUATION WAS PERFORMED. A REVIEW OF THE DEVICE HISTORY RECORD FOR LOT NUMBER 7614731 INDICATED NO NON-CONFORMANCES. A REVIEW OF OUR COMPLAINT MANAGEMENT SYSTEM REVEALED THIS TO BE THE ONLY COMPLAINT ASSOCIATED WITH THIS LOT NUMBER. THE APPROPRIATE MANUFACTURING DOCUMENTS FROM THE DEVICE MASTER RECORD (DMR) PERTAINING TO THE REPORTED FAILURE MODE WERE REVIEWED, REVEALING NO NOTABLE GAPS IN THE MANUFACTURING PROCESS. TRAINED PRODUCTION PERSONNEL PREPPING AND FILLING THE VIAL WITH POLYVINYL ALCOHOL (PVA) ARE REQUIRED TO WERE PROPER ATTIRE IN ORDER TO PREVENT CONTAMINATING THE PVA. THE PARTICLES AND VIAL ARE INSPECTED MULTIPLE TIMES TO CONFIRM EACH VIAL IS FREE OF FOREIGN MATTER AND HAS A COMPLETE SEAL. EACH DEVICE IS SHIPPED WITH INSTRUCTIONS FOR USE (IFU) LISTING THE INDICATIONS FOR USE, CONTRAINDICATIONS, WARNINGS AND PRECAUTIONS, AND THE CORRECT DEPLOYMENT PROCEDURE. T_PVA_REV8 [POLYVINYL ALCOHOL FOAM EMBOLIZATION PARTICLES] STATES: PRECAUTIONS: SMALL CONTAMINATING PARTICLES FOUND ON THE ANGIOGRAPY TABLE MAY CAUSE FOREIGN BODY REACTIONS OR ACTUAL INFECTION. THE PHYSICIAN SHOULD USE THE UTMOST CAUTION TO AVOID CONTAMINANTS DURING PREPARATION OF THE DEVICE FOR USE. USE OF ANGIOGRAPY FOR PREOPERATIVE EVALUATION, OPERATIVE CONTROL AND POSTOPERATIVE FOLLOW-UP IS RECOMMENDED. AS WITH ANY SURGICAL PROCEDURE, STRICT ATTENTION TO STERILE TECHNIQUE IS REQUIRED. POTENTIAL ADVERSE EFFECTS: FOREIGN BODY REACTIONS NECESSITATING MEDICAL INTERVENTION. HOW SUPPLIED: STERILE IF PACKAGE IS UNOPENED OR UNDAMAGED. DO NOT USE THE PRODUCT IF THERE IS DOUBT AS TO WHETHER THE PRODUCT IS STERILE. STORE IN A DARK, DRY, COOL PLACE. AVOID EXTENDED EXPOSURE TO LIGHT. UPON REMOVAL FROM PACKAGE, INSPECT THE PRODUCT TO ENSURE NO DAMAGE HAS OCCURRED. DISCARD ANY UNUSED MATERIALS AFTER USE. DO NOT RE-STERILIZE.¿ PER CUSTOMER TESTIMONY AND THE DEVICE FAILURE ANALYSIS, IT IS EVIDENT THAT A FOREIGN SUBSTANCE WAS INSIDE THE VIAL, CAUSING THE PVA TO BECOME CONTAMINATED. HOWEVER, IT CANNOT BE DETERMINED HOW THE FOREIGN SUBSTANCE WAS INTRODUCED INTO THE VIAL. THUS, THE ROOT CAUSE OF THIS COMPLAINT WILL BE TRENDED AS ¿INCONCLUSIVE¿. THIS FAILURE MODE HAS BEEN ESCALATED PER INTERNAL PROCESSES. WE WILL CONTINUE TO MONITOR FOR SIMILAR COMPLAINTS AND HAVE NOTIFIED THE PROPER PERSONNEL ABOUT THIS EVENT. PER THE RISK ASSESSMENT NO FURTHER ACTION IS REQUIRED.

    Description of Event or Problem · 1

    THE INTERNATIONAL CUSTOMER REPORTED THAT, UPON INSPECTION OF THE DEVICE FOR A BRONCHIAL ARTERY EMBOLIZATION PROCEDURE, RED COLORED FOREIGN MATTER OF AN UNKNOWN ORIGIN WAS FOUND INSIDE THE PRODUCT VIAL. THE CUSTOMER REFUSED TO USE THE PRODUCT ON ACCOUNT OF THE FOREIGN MATTER. THIS OBSERVATION WAS MADE PRIOR TO CONTACT WITH A PATIENT; ACCORDINGLY, NO PATIENT ADVERSE EVENTS RESULTED FROM THE PRODUCT PROBLEM. THE COMPLAINT PRODUCT HAS BEEN RETURNED TO THE MANUFACTURER; HOWEVER, AS OF THE DATE OF THIS REPORT, THE EVALUATION AND INVESTIGATION ARE ONGOING. NO FURTHER INFORMATION REGARDING THE INCIDENT WAS PROVIDED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    215208 PVA FOAM EMBOLIZATION PARTICLES KRD COOK INC N/A 00827002096653

    Patients

    Seq Age Sex Outcome Treatment
    1 60 YR