"Becton Dickinson (BD) CareFusion 303 Inc. Recalls Alaris™ Syringe and Alaris™ PCA Modules Due to Potential Incorrect Display of Syringe Types and/or Sizes" FDA (2020).
BD/Carefusion 303 is recalling the Alaris™ Syringe Module and Alaris™ PCA Module because the Alaris PC units may display the incorrect syringe types and/or sizes. This could potentially result in delays in infusion, under-infusion, or over-infusion. If this occurs, this could lead to serious adverse events, including death.
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