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Compatibility Issues Prompt Recall of Alaris Infusion Pumps

Becton Dickinson (BD)/Carefusion 303 has voluntarily recalled the Alaris infusion pump due to incompatibility issues.

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BD recalls more Alaris pumps due to syringe compatibility issues

The FDA determined that another recall of BD Alaris infusion pumps is Class I, the most serious kind.

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Eitan infusion pumps join Baxter, B Braun in spate of recalls

Eitan infusion pumps join Baxter, B Braun in spate of recalls
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Health News Roundup: US FDA says BD recalling infusion pumps due to compatibility issues; AstraZeneca, AI biologics firm Absci tie up on cancer drug and more

Health News Roundup: US FDA says BD recalling infusion pumps due to compatibility issues; AstraZeneca, AI biologics firm Absci tie up on cancer drug and more
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US FDA says BD is recalling infusion pumps due to compatibility issues

The U.S. Food and Drug Administration (FDA) said on Friday that Becton Dickinson is recalling its Alaris infusion pumps due to compatibility issues with Cardinal Health's Monoject syringes. The health regulator said Alaris pumps are validated for use with Monoject syringes. However, the dimensions for Monoject syringes have recently changed while rebranding the syringes from Covidien Monoject to Cardinal Health Monoject.

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