OFFICIAL-SOURCE RECALL · CANADA
Patient Information Centre iX Recall: ous situation occurs if the observed behavior is
Use the identifiers printed on your item to determine whether this recall may affect the product you own.
CHECK THE ITEM YOU OWN
Is your product affected?
- Brand
- See official notice
- Product
- Patient Information Centre iX
- Manufacturer
- See official notice
The barcode may identify the product type, while the recall may apply only to certain lots, dates or variants. Check all identifiers listed in the official recall.
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
Read the official CANADA_MEDICAL_DEVICES recall notice →SCAN ONCE. KEEP WATCHING.
Keep an eye on the products at home.
Scan food and household product barcodes, save your items and get notified when a future recall may match.
