OFFICIAL-SOURCE RECALL · CANADA
Patient Information Centre iX Recall: ous situation occurs if the observed behavior is
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- Brand
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Why this product was recalled
ous situation occurs if the observed behavior is: Loss of central alarming, Loss of, or frozen, waveforms/data display -Bedside monitors and telemetry devices could generate a "No Central Mon" INOP Additional information Details Original
Hazard
ous situation occurs if the observed behavior is: Loss of central alarming, Loss of, or frozen, waveforms/data display -Bedside monitors and telemetry devices could generate a "No Central Mon" INOP Additional information Details Original
Official recall notice
Patient Information Centre iX
Agency: Health Canada
Official publication date: August 20, 2026
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