Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.
Reason for recall: Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood. Distribution: Worldwide distribution - US Nationwide and the country of Canada. Quantity: 47370 units Lot/code info: UDI-DI 04046964837821; All Lots Distributed After 01AUG2023.
04046964837821
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.