BEUDAMED
    FDA Enforcement Class II Ongoing

    11272VN 11272VNK Flexible Video Urethro Cystoscope Z18442US-BD (08/2018); 11272VNU 11272VNUK Flexible Video Urethro Cystoscope Z18442US-BD (08/2018)

    Recall: Z-1064-2022 · Reported May 18, 2022

    Enforcement

    Recall Number
    Z-1064-2022
    Event ID
    89880
    Classification
    Class II
    Status
    Ongoing
    Product Type
    Devices
    Firm
    Karl Storz Endoscopy
    Voluntary / Mandated
    Voluntary: Firm initiated
    Initial Notification
    Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
    Report Date
    May 18, 2022
    Initiation Date
    April 1, 2022
    Classification Date
    May 12, 2022
    Address
    2151 E Grand Ave, N/A, El Segundo, CA, 90245-5017, United States

    Description

    11272VN 11272VNK Flexible Video Urethro Cystoscope Z18442US-BD (08/2018); 11272VNU 11272VNUK Flexible Video Urethro Cystoscope Z18442US-BD (08/2018)

    Reason

    Failure to achieve the expected six-log reduction in microorganisms following the disinfection process.

    Code Info

    11272VN 11272VNK Flexible Video Urethro Cystoscope Z18442US-BD (08/2018) UDI Code: 4048551226186; 11272VNU 11272VNUK Flexible Video Urethro Cystoscope Z18442US-BD (08/2018) UDI Code: 4048551226193; All Serial Numbers manufactured/distributed since January 2018.

    Distribution

    U.S.: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, Guam, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA,WI, WV, and WY. O.U.S.: Mexico, Lebanon, and South Korea

    Quantity

    All Serial Numbers manufactured/distributed since January 2018