BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PROMUS PREMIER SELECT

    MDR report key: 18941968 · Received March 20, 2024

    Report

    Report Number
    2124215-2024-16918
    Event Type
    Malfunction
    Date Received
    March 20, 2024
    Date of Event
    February 24, 2024
    Report Date
    April 12, 2024
    Manufacturer
    BOSTON SCIENTIFIC CORPORATION
    Product Code
    NIQ
    Removal / Correction Number
    97172244-FA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GM
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Additional Manufacturer Narrative · 0

    DEVICE HISTORY RECORD REVIEW: THE BATCH NUMBER WAS NOT PROVIDED. A SHIP HISTORY WAS PERFORMED WHICH IDENTIFIED THREE POTENTIAL BATCHES. ONE OF THESE BATCHES WAS IDENTIFIED AS BEING BATCH 31891839. A DEVICE HISTORY RECORDS (DHR) REVIEW WAS PERFORMED FOR THE PROMUS PREMIER SELECT REFERENCED BATCH (0031891839). THE MANUFACTURING REVIEW CONFIRMED THAT ALL DEVICES ASSOCIATED WITH THIS BATCH WERE THE CORRECT SIZE (16 MM X 2.75 MM) PER MANUFACTURING RECORDS AND BOX LABELLING. THE PROMUS PREMIER SELECT 16 MM X 2.75 MM HAS A MINIMUM STENT LENGTH SPECIFICATION OF 15.71 MM, AND A MAXIMUM STENT LENGTH SPECIFICATION OF 17.21 MM. ANY STENT LENGTH THAT FALLS OUTSIDE OF THESE LIMITS IS AUTOMATICALLY SCRAPPED. ALL DISTRIBUTED DEVICES FROM FINISHED GOODS BATCH (FGB) 0031891839 PASSED THIS INSPECTION AND WERE WITHIN THE SPECIFIED STENT LENGTH LIMITS. FROM THE THOROUGH INVESTIGATION OF ALL DATA GATHERED, IT IS NOT POSSIBLE FOR A FGB OF 16 MM X 2.75 MM DEVICES TO INCLUDE A 20 MM X 4.00 MM SIZED DEVICE. DEVICE ANALYSIS: THE PROMUS PREMIER SELECT DEVICE WAS NOT RETURNED FOR ANALYSIS AND WAS DISCARDED. LABELING REVIEW: BASED ON THE AVAILABLE INFORMATION, THERE WAS NO EVIDENCE OF DEVICE MISUSE, OFF-LABEL USE, OR FAILURE TO FOLLOW THE PROMUS PREMIER SELECT CORONARY STENT SYSTEM INSTRUCTIONS FOR USE (IFU). INVESTIGATION CONCLUSION: BASED ON A THOROUGH REVIEW OF THE REPORTED EVENT, BOSTON SCIENTIFIC HAS ASSIGNED AN INVESTIGATION CONCLUSION CODE OF 'MANUFACTURING DEFICIENCY', SINCE THE PROBLEM WAS TRACED TO THE MANUFACTURING PROCESS. ALTHOUGH THE ACTUAL DEVICE ASSOCIATED WITH THIS COMPLAINT WAS NOT RETURNED FOR ANALYSIS, AN ANALYSIS INTO OTHER DEVICES FROM THIS BATCH (31891839) CONFIRMED A MISPRINT ON THE HUB MANIFOLDS. THE PRINT SIZE ON THE HUB WAS A 4.00X20MM, HOWEVER THE THE DEVICE WAS LABELLED AS A 16MM X 2.75 PROMUS PREMIER SELECT. AN NCEP INVESTIGATION HAS BEEN INITIATED TO IDENTIFY THE CAUSE OF THE INCORRECT PRODUCT SIZE ETCHED ON THE HUB MANIFOLDS FROM THIS BATCH (0031891839). IN ADDITION, BOSTON SCIENTIFIC INITIATED A MEDICAL DEVICE REMOVAL (97172244-FA) OF BATCH 0031891839 OF PROMUS PREMIER SELECT CORONARY STENT SYSTEMS ON 11 MARCH 2024 DUE TO AN INCORRECT PRODUCT SIZE PRINTED ON THE CATHETER MANIFOLD HUB.

    Description of Event or Problem · 0

    IT WAS REPORTED THAT A STENT LABELING ISSUE OCCURRED. A 16 MM X 2.75 MM PROMUS PREMIER SELECT CORONARY STENT SYSTEM WAS SELECTED FOR USE TO TREAT A TARGET LESION. DURING PREPARATION, IT WAS NOTED THE STENT DISPLAYED THE SIZE OF 20 MM X 4.0 MM. A REPLACEMENT 16 MM X 2.75 MM PROMUS PREMIER SELECT CORONARY STENT SYSTEM WAS USED TO COMPLETE THE PROCEDURE. NO PATIENT COMPLICATIONS WERE REPORTED.

    Description of Event or Problem · 0

    IT WAS REPORTED THAT A STENT LABELING ISSUE OCCURRED. A 16 MM X 2.75 MM PROMUS PREMIER SELECT CORONARY STENT SYSTEM WAS SELECTED FOR USE TO TREAT A TARGET LESION. DURING PREPARATION, IT WAS NOTED THE STENT DISPLAYED THE SIZE OF 20 MM X 4.0 MM. A REPLACEMENT 16 MM X 2.75 MM PROMUS PREMIER SELECT CORONARY STENT SYSTEM WAS USED TO COMPLETE THE PROCEDURE. NO PATIENT COMPLICATIONS WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    455148 PROMUS PREMIER SELECT STENT, CORONARY, DRUG-ELUTING NIQ BOSTON SCIENTIFIC CORPORATION 10663

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown