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Displaying 1 - 3 of 3 items.
BD Alaris™ Infusion Devices
BD is issuing a notification to inform customers that Cardinal Health branded Monoject™ syringes have not been validated for use with the BD Alaris™ infusion devices. BD has validated Covidien branded Monoject™ syringes for use with the BD Alaris™…
RecallHealth product recall | 2023-10-30
BD Alaris Large Volume Pump
BD is recalling the product because if a third-party screw is used, or potentially if the BD manufactured pivot latch screw is reused or improperly installed, it may back out, interfering with door closure, which can lead to over or under infusion. The…
RecallHealth product recall | 2022-12-01
Bd Alaris
Recall is being initiated to notify customers to the risk of the use and installation of unauthorized, third-party parts on the Alaris system.
Recall start date: Feb 7, 2022
RecallHealth product recall | 2022-02-28