Health Canada — Medical Devices · Canada · 2020-07-17 · Type II
🏛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 →
Reported risk: Recall is being initiated to notify customers of the following four hardware situations that require user attention and actions: damaged inter-unit-interface (IUI) connectors, broken elements on the Alaris Pump Module platen, improperly secured PC unit battery, and dim segment.
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.
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