Raanana, Israel
Medimop Medical Projects Ltd. recalls
1 recall recorded since 2018, most recently on 6 October 2017. None are listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)0
Terminated or completed1
Class I (FDA)0
Terminated Class II Medical devices
- Recall started
- 6 October 2017
- Terminated
- 23 January 2024
- Reason
- 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.
- Distribution
- US Distribution
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-0972-2018
- 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.
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.