BEUDAMED
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    MEDIMOP 20MM VIAL ADAPTER

    FDA Adverse Event
    Death ·MEDIMOP MEDICAL PROJECTS, LTD.·Product code LHI·December 4, 2014

    MIXJECT TRANSFER DEVICE

    FDA Adverse Event
    Injury ·MEDIMOP MEDICAL PROJECTS, LTD.·Product code LHI·September 1, 2011

    MIXJECT TRANSFER DEVICE

    FDA Adverse Event
    Death ·MEDIMOP MEDICAL PROJECTS, LTD.·Product code LHI·December 19, 2012

    MIXJECT TRANSFER DEVICE

    FDA Adverse Event
    Injury ·MEDIMOP MEDICAL PROJECTS, LTD.·Product code LHI·December 19, 2012

    MIXJECT TRANSFER DEVICE

    FDA Adverse Event
    Injury ·MEDIMOP MEDICAL PROJECTS, LTD.·Product code LHI·July 1, 2013

    20MM VIAL ADAPTER

    FDA Adverse Event
    Death ·MEDIMOP MEDICAL PROJECTS, LTD.·Product code LHI·December 17, 2013

    VIAL2BAG DC

    FDA Adverse Event
    Malfunction ·MEDIMOP MEDICAL PROJECTS LTD.·Product code LHI·March 23, 2018

    VIAL ADAPTOR

    FDA Adverse Event
    Malfunction ·MEDIMOP MEDICAL PROJECTS LTD.·Product code LHI·March 30, 2018

    VIAL2BAG DC

    FDA Adverse Event
    Malfunction ·MEDIMOP MEDICAL PROJECTS LTD.·Product code LHI·March 16, 2018

    VIAL2BAG DC

    FDA Adverse Event
    Malfunction ·MEDIMOP MEDICAL PROJECTS LTD.·Product code LHI·March 23, 2018

    VIAL2BAG DC 20MM

    FDA Adverse Event
    Malfunction ·MEDIMOP MEDICAL PROJECTS LTD.·Product code LHI·May 15, 2018

    Crosseal, fibrin sealant (human), This package***, One Applicator, Two Vial cups, Sterile, Disposable, Single Use, For Usage***, Rx Only, Distributed by American Red Cross Blood Services, Washington, DC 20006, Manufactured by: Medimop Medical Projects Ltd, for OMRIX biopharmaceuticals, Utd, MDA blood bank, Sheba Hospital, Romat-Gan, PO8 888, Kiryat Ono 55000 Israel

    FDA Recall
    Terminated ·Omrix Biopharmaceuticals, Ltd. Plasma Fract. Inst. Magen David Adom Blood Services Ctr., Sheba Hospital Ramat Gan Israel·Product code FMF·August 6, 2004

    VIAL2BAG DC

    FDA Adverse Event
    Malfunction ·MEDIMOP MEDICAL PROJECTS LTD (WEST PHARMACEUTICAL SERVICES·Product code LHI·May 22, 2018

    Vial2BagDC, Product Number 6070112. The 20mm Vial2Bag DC device, is intended for use in healthcare facilities or in-home environment by the patient or care-giver to aid and support prescribed treatment and therapy. The device consists of the Vial2Bag piercing spike and cover, the IV Port connector and an integrated Vial Adapter (20mm) for access to the drug/solution vial.

    FDA Recall
    Terminated ·Medimop Medical Projects Ltd.·Product code LHI·October 6, 2017

    MIX2VIAL

    FDA Adverse Event
    Malfunction ·MEDIMOP MEDICAL PROJECTS LTD. / WEST PHARMACEUTICAL SERVICES INC.·Product code LHI·December 27, 2018

    Vial2BagDC, Product Number 6070112. The 20mm Vial2Bag DC device, is intended for use in healthcare facilities or in-home environment by the patient or care-giver to aid and support prescribed treatment and therapy. The device consists of the Vial2Bag piercing spike and cover, the IV Port connector and an integrated Vial Adapter (20mm) for access to the drug/solution vial.

    FDA Enforcement
    Class II ·Terminated·Medimop Medical Projects Ltd.·March 21, 2018