BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE

    MDR report key: 790101 · Received November 21, 2006

    Report

    Report Number
    2023826-2006-01783
    Event Type
    Malfunction
    Date Received
    November 21, 2006
    Report Date
    October 23, 2006
    Manufacturer
    STAAR SURGICAL CO.
    Product Code
    HQL
    PMA / PMN Number
    P990013
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AZ, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    H6: EVALUATION CODES: RESULTS - (OTHER) VISUAL INSPECTION OF THE RETURNED PRODUCT FOUND THE LENS OPTIC TORN. THERE WAS EVIDENCE OF CLEAR SURGICAL RESIDUE. CONCLUSION - (OTHER): BASED ON THE COMPLAINT HISTORY AND THE EVALUATION OF THE RETURNED PRODUCT, A SPECIFIC ROOT CAUSE OF THE EVENT COULD NOT BE DETERMINED. IT SHOULD BE NOTED THAT THE INJECTOR AND CARTRIDGE WERE NOT RETURNED FOR EVAL.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE SURGEON INSERTED A CQ2015 COLLAMER THREE PIECE LENS AND THE HAPTIC TORE. THE LENS WAS REMOVED WITH NO PT INJURY. ADDITIONAL INFO HAS BEEN REQUESTED, BUT TO DATE NONE HAS BEEN FORTHCOMING. IF ADD'L INFO IS REC'D, A SUPPLEMENTAL MEDWATCH WILL BE SENT. THIS IS ONE OF FOUR LENSES USED ON THIS PT - SEE MFR REPORT # 2023826-2006-01781, # 2023826-2006-01782 AND # 2023826-2006-01784.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE INTRAOCULAR LENS HQL STAAR SURGICAL CO. CQ2015 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN CARTRIDGE MODEL CQ CARTRIDGE -FP - LOT NUMBER UNK| INJECTOR MODEL MSI-PM - LOT NUMBER UNK