BEUDAMED
    FDA Enforcement Class II Terminated

    XP-CR Tibial Tray - Interlok 79 mm Item # 195276

    Recall: Z-2511-2019 · Reported September 18, 2019

    Enforcement

    Recall Number
    Z-2511-2019
    Event ID
    83594
    Classification
    Class II
    Status
    Terminated
    Product Type
    Devices
    Firm
    Zimmer Biomet, Inc.
    Voluntary / Mandated
    Voluntary: Firm initiated
    Initial Notification
    Letter
    Report Date
    September 18, 2019
    Initiation Date
    August 15, 2019
    Classification Date
    September 12, 2019
    Termination Date
    April 16, 2021
    Address
    56 E Bell Dr, Warsaw, IN, 46582-6989, United States

    Description

    XP-CR Tibial Tray - Interlok 79 mm Item # 195276

    Reason

    The locking bar not fully engaging

    Code Info

    Lot Number 663820 503480 262450 308140 308150 473010 513130 320340 320590 579060 571060 938200 322150 066240 283270 322200 851360 996030 996030R 090250 841560 206870 322180 258110 279270 553900 711510 161980 161990 274450 043940 041260 663840 041170 993800 883570 883600 883590 883580 888420 374120 599170 576060 279060 712600 576050 672660 821370 600820 717210 943420 221180 141500 199770 450380 220060 502880 513120

    Distribution

    State NY IN OH MI GA SC FL MO WI MN ND SD NE NJ PA MD IL IA CA VA NC DC WV AR AL MS AL MI WA OR ID LA FL KS TN MA KY OK TX TX CT AZ NV NM MT WY CO UT DC WY Country: KOREA CHINA CANADA AUSTRALIA JAPAN EMEA SWEDEN ITALY

    Quantity

    319 units