Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Vial2BagDC Recalled by Medimop Medical Projects Ltd. Due to Medimop is recalling certain lots of this product...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Medimop Medical Projects Ltd. directly.
Affected Products
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.
Quantity: 453,600 units
Why Was This Recalled?
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.
Where Was This Sold?
US Distribution
About Medimop Medical Projects Ltd.
Medimop Medical Projects Ltd. has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report