BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    HD AUTOCLAVABLE CAMERA HEAD

    MDR report key: 12306489 · Received August 11, 2021

    Report

    Report Number
    8010047-2021-10082
    Event Type
    Malfunction
    Date Received
    August 11, 2021
    Date of Event
    July 15, 2021
    Report Date
    February 23, 2022
    Manufacturer
    OLYMPUS MEDICAL SYSTEMS CORP.
    Product Code
    FET
    PMA / PMN Number
    K955404
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AS
    Reporter Occupation
    OTHER
    Health Professional
    N

    Narratives

    Additional Manufacturer Narrative · 0

    THIS SUPPLEMENTAL REPORT IS BEING SUBMITTED TO PROVIDE THE SUBJECT DEVICE EVALUATION RESULT. THE SUBJECT DEVICE WAS RETURNED TO OLYMPUS AUSTRALIA AND NEW ZEALAND (OAZ) FOR EVALUATION. OLYMPUS MEDICAL SYSTEMS CORP. (OMSC) REVIEWED THE DEVICE HISTORY RECORD (DHR) OF THE SUBJECT DEVICE AND CONFIRMED NO IRREGULARITY. BASED UPON THE INFORMATION FROM OAZ, OMSC SURMISED THAT THE REPORTED PHENOMENON WAS ATTRIBUTED TO THE FAILURE OF THE VIDEO COMMUNICATION TO THE PROCESSOR DUE TO THE FAILURE OF THE CABLE BY THE USER HANDLING. OLYMPUS STATED THE APPROPRIATE HANDLING OF OTV-S7PROH-HD-10E AND THE COUNTER MEASURES AGAINST ABNORMALITIES IN THE INSTRUCTION MANUAL OF OTV-S7PROH-HD-10E.

    Additional Manufacturer Narrative · 1

    THE SUBJECT DEVICE WAS NOT RETURNED TO OMSC FOR EVALUATION BUT WAS RETURNED TO OLYMPUS AUSTRALIA AND (B)(4). CHECKED THE SUBJECT DEVICE AND FOUND THAT THE REPORTED PHENOMENON WAS DUPLICATED. WHEN USING OTHER CABLE ASSEMBLY, THE IMAGE APPEARED. THE EXACT CAUSE OF THE REPORTED EVENT COULD NOT BE CONCLUSIVELY DETERMINED AT THIS TIME. IF ADDITIONAL INFORMATION IS RECEIVED, THIS REPORT WILL BE SUPPLEMENTED.

    Description of Event or Problem · 1

    OLYMPUS MEDICAL SYSTEMS CORP. (OMSC) WAS INFORMED FROM THE USER THAT DURING MAINTENANCE, IT WAS FOUND THAT THE ENDOSCOPIC IMAGE WAS NOT DISPLAYED, ONLY COLOR BAR WAS DISPLAYED. THERE WAS NO REPORT OF PATIENT INJURY ASSOCIATED WITH THE EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1207304 HD AUTOCLAVABLE CAMERA HEAD CAMERA HEAD FET OLYMPUS MEDICAL SYSTEMS CORP. OTV-S7PROH-HD-10E

    Patients

    Seq Age Sex Outcome Treatment
    1 Unknown