Medimop Medical Projects Ltd.: Medical Device Recall in 2018 - (Recall #: Z-0972-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class II

Date Initiated: October 6, 2017

Date Posted: March 21, 2018

Recall Number: Z-0972-2018

Event ID: 79243

Reason for Recall:

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.

Status: Terminated

Product Quantity: 453,600 units

Code Information:

Lots: 9507,9508,9509,9510,9511,9512,9513.

Distribution Pattern:

US Distribution

Voluntary or Mandated:

Voluntary: Firm initiated