Health Canada — Marketed Health Products · Canada · 2010-10-14
As described by Health Canada — Marketed Health Products: Alaris PC unit (model 8000) - Total Bolus Display Error - Notice to Hospitals
🏛Compiled from an official source — the facts on this page are reproduced from the issuing authority’s own published notice, which is linked above. No AI-generated text appears on this page. How we use AI →
Archived by the issuing authority — kept for reference
Reported risk: To Alaris ® System users, Required Action for Users: Warning Tag: The model 8000 PC unit, when used with an Alaris Pump module or Alaris Syringe module may under certain conditions display an incorrect total dose when programmed to deliver a bolus dose. The Alaris Pump module or Alaris Syringe module delivers the actual programmed bolus dose (and associated volume to be infused) regardless of the displayed total bolus dose.
Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.
ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.