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Medimop Medical Projects Ltd. recalls Vial2BagDC, Product Number 6070112. The 20mm Vial2Bag DC device, is intended for use in healthcare facilities or in-h
Recalled March 21, 2018 · FDA recall Z-0972-2018 · Medimop Medical Projects
Hazard
Medimop is recalling certain lots of this product Vial2Bag DC due to the potential of the IV Port separating from the Via12Bag DC body during the drug reconstitution I IV Set attachment process. · FDA Class II
Units
453,600 units
Sold at
US Distribution
Description
Medimop is recalling certain lots of this product Vial2Bag DC due to the potential of the IV Port separating from the Via12Bag DC body during the drug reconstitution I IV Set attachment process.
Product
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.
Manufacturer(s)
Medimop Medical Projects Ltd.
Made in
Israel
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →