Voluntary Recall for Cardinal Well being Model Monoject™ Sterile Syringes – The Journal of Healthcare Contracting

Voluntary Recall for Cardinal Well being Model Monoject™ Sterile Syringes – The Journal of Healthcare Contracting



February 5, 2024 – In shut coordination with the U.S. Meals and Drug Administration (FDA), Cardinal Well being has issued a voluntary product removing of Cardinal Well being Model Monoject™ Luer-Lock Sterile Syringes in all sizes (1, 3, 6, 12, 20 , 35 and 60 ml) and Cardinal Well being model Monoject™ enteral sterile syringes with the ENFit™ connection (1, 3, 6, 12, 35 and 60 ml), that are coloured purple to point enteral feeding solely.

This product removing is lot particular and applies to all Cardinal Well being model Monoject™ sterile syringes described under. Covidien model Monoject™ syringes in all sizes usually are not affected by this product promotion. Prospects who buy customized Presource kits containing affected parts will likely be notified of the removing of this product through a separate letter.

When used with a pump, the Cardinal Well being Model Monoject™ Sterile Syringe will not be acknowledged by the pump, which can lead to delays in remedy or remedy. Conversely, if the syringe is acknowledged by pumping, this will lead to variations in quantity and/or infusion fee, which can result in over or underneath infusion. Though we now have not obtained any stories of affected person deaths on account of impacted syringes, there’s a potential danger of significant harm or demise.

Study extra from Cardinal Well being

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