BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TECNIS ITEC PRELOADED 1-PIECE IOL

    MDR report key: 7262691 · Received February 11, 2018

    Report

    Report Number
    2648035-2018-00229
    Event Type
    Malfunction
    Date Received
    February 11, 2018
    Date of Event
    January 11, 2018
    Report Date
    May 17, 2018
    Manufacturer
    ABBOTT MEDICAL OPTICS
    Product Code
    HQL
    UDI-DI
    05050474558502
    PMA / PMN Number
    P980040
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UK
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE INTRAOCULAR LENS WAS REMOVED AND REPLACED DURING THE SAME PROCEDURE. (B)(6). ALL PERTINENT INFORMATION AVAILABLE TO ABBOTT MEDICAL OPTICS HAS BEEN SUBMITTED.

    Additional Manufacturer Narrative · 1

    ADDITIONAL INFORMATION: AGE/DATE OF BIRTH: (B)(6). SEX/GENDER: FEMALE. DATE OF EVENT: (B)(6) 2018. DURING FOLLOW UP IT WAS REPORTED THAT A WHITE BLEMISH NOTICED ON OPTIC. THE LENS WAS REMOVED AND REPLACED WITHOUT HARM TO THE PATIENT. VISUAL ACUITY PRE-OP 6/60 U/A (B)(6) 2018. VISUAL ACUITY POST-OP 0.90 U/A (B)(6) 2018 (AMBLIOPIC EYE). THERE WAS NO SECONDARY SURGICAL INTERVENTION REQUIRED. ALL PERTINENT INFORMATION AVAILABLE TO JOHNSON AND JOHNSON SURGICAL VISION, INC. HAS BEEN SUBMITTED.

    Additional Manufacturer Narrative · 1

    DEVICE AVAILABLE FOR EVALUATION, RETURNED TO MANUFACTURER ON: 03/23/2018. DEVICE EVALUATION: THE SAMPLE WAS RECEIVED IN A PLASTIC BAG. THE PLUNGER WAS OBSERVED IN ADVANCED POSITION AND LOCK. THE CARTRIDGE WAS CORRECTLY ENGAGED INTO THE DEVICE. NO ASSEMBLY ERROR AND/OR DEFECT RELATED TO MANUFACTURING PROCESS WERE OBSERVED. THE LENS WAS RECEIVED IN SOLUTION IN SAMPLE CONTAINER. VISUAL INSPECTION AT 10X MICROSCOPE MAGNIFICATION WAS PERFORMED; LACK OF LUBRICANT MATERIAL WAS OBSERVED IN THE DEVICE AND WHITE FOREIGN BODY WAS OBSERVED ON THE OPTIC OF THE IOL. THE SAMPLE WAS SENT TO AN OUTSIDE LABORATORY FOR FURTHER ANALYSIS. VISUAL APPEARANCE, SCANNING ELECTRON MICROSCOPE (SEM) AND ENERGY DISPERSIVE X-RAY (EDX) ANALYSIS SHOW THAT THE WHITE DEBRIS IS CONSISTENT WITH A MIXTURE OF TITANIUM DIOXIDE(WIDELY USED WHITE PIGMENT) AND ALUMINOSILICATES (¿DIRT¿). BASED ON THE SUBJECT MATTER EXPERT (SME) EVALUATION, A WHITE COLORED FLAKE TYPE OF PARTICLE WAS OBSERVED SIMILAR IN COLOR TO THE ONE UTILIZED IN MANUFACTURING THE PLUNGER AND THE NUT COMPONENTS OF THE DEVICE. THERE IS POSSIBILITY THAT DURING HANDLING OF THE DEVICE. A SMALL PARTICLE COULD HAVE BEEN PEELED OR DETACHED FROM THE DEVICE. HOWEVER, THIS IS UNLIKELY EVENT GIVEN THE FACT THAT THERE WAS NO IOL CONTACT BETWEEN THE PLUNGER AND NUT COMPONENTS. IN ADDITION TO MANUFACTURING PROCESS, THERE ARE VARIOUS CLEANING AND INSPECTION POINTS IN WHICH 100% VISUAL INSPECTION IS PERFORMED TO ASSURE THAT THE LENS IS IN GOOD CONDITION BEFORE IT IS PLACED IN THE PCB00 DEVICE SYSTEM. THERE ARE ALSO 100% VISUAL INSPECTION DURING THE ASSEMBLY PROCESS OF THE DEVICE TO ASSURE LENS IS SEATED BEHIND THE BUMPS OF THE LOWER BODY IN LENS STORAGE AREA. THE REPORTED ISSUE WAS VERIFIED. HOWEVER, THE CONDITION IN WHICH THE SAMPLE WAS RETURNED IS CONSISTENT WITH A PRODUCT THAT WAS HANDLED AND PREPARED FOR SURGICAL PROCESS. BASED ON THE ANALYSIS THERE IS NO INDICATION OF PRODUCT QUALITY DEFICIENCY. MANUFACTURING RECORD REVIEW: MANUFACTURING RECORD REVIEW OF THE PRODUCTION ORDER AND RELATED DOCUMENT REVEALED THAT THE PRODUCT WAS MANUFACTURED AND RELEASED ACCORDING TO SPECIFICATION. THERE WAS NO DISCREPANCY FOUND DURING THE REVIEW. A SEARCH REVEALED THAT NO OTHER COMPLAINT WAS RECEIVED FROM THIS PRODUCTION ORDER. LABELING REVIEW: THE DIRECTIONS FOR USE (DFU) WAS REVIEWED. THE DFU ADEQUATELY PROVIDES INSTRUCTIONS AND PRECAUTIONS FOR THE PROPER USE AND HANDLING OF THE PRODUCT. CONCLUSION: BASED ON THE INVESTIGATION, RESULTS THERE IS NO INDICATION OF A PRODUCT QUALITY DEFICIENCY. ALL PERTINENT INFORMATION AVAILABLE TO JOHNSON & JOHNSON SURGICAL VISION, INC. HAS BEEN SUBMITTED.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE INTRAOCULAR LENS (IOL) HAD A FOREIGN BODY ON IT. DURING FOLLOW UP IT WAS REPORTED THAT THE FOREIGN MATERIAL LOOKED LIKE A FLECK ON THE IOL. THE ISSUE WAS NOTICED UPON IMPLANTATION. THE IOL WAS REMOVED AND REPLACED. ANOTHER IOL WAS SUCCESSFULLY IMPLANTED. IT IS NOT BELIEVED THAT THERE WAS ANY INJURY TO THE PATIENT. NO ADDITIONAL INFORMATION WAS PROVIDED TO ABBOTT MEDICAL OPTICS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    105964 TECNIS ITEC PRELOADED 1-PIECE IOL MONOFOCAL IOLS HQL ABBOTT MEDICAL OPTICS PCB00 05050474558502

    Patients

    Seq Age Sex Outcome Treatment
    1 78 YR