Health Canada — Medical Devices · Canada · 2020-08-28 · Type II
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Reported risk: Recall is being initiated to notify customers that the damage to the syringe barrel clamp mechanism on either the Alaris Syringe Module or Alaris PCA Module may result in the Alaris PC Unit displaying incorrect syringe types and/or sizes and that this issue could potentially result in delays in infusion, under-infusion, or over-infusion.
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