LIFEPAK ® 35 Monitor/Defibrillator
OFFICIAL-SOURCE RECALL · CANADA
LIFEPAK ® 35 Monitor/Defibrillator Recall: Stryker has identified an issue with the LP35 where
Use the identifiers printed on your item to determine whether this recall may affect the product you own.
CountryCanadaPublishedSeptember 2, 2026Last updatedSeptember 2, 2026Official source last checkedSeptember 4, 2026 at 1:39 PM UTC
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Is your product affected?
- Brand
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- Product
- LIFEPAK ® 35 Monitor/Defibrillator
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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
Stryker has identified an issue with the LP35 where the device does not display the message "CHECK RHYTHM / ECG Analysis Inconclusive" as intended when specific conditions are present simultaneously. The issue does not affect the display of "shock advised" or "no shock advised" messages, and therapy delivery remains available. Additionally, this nonconformance is limited to the device on-screen prompts only; rhythm analysis is not impacted by this issue.
Hazard
Stryker has identified an issue with the LP35 where the device does not display the message "CHECK RHYTHM / ECG Analysis Inconclusive" as intended when specific conditions are present simultaneously. The issue does not affect the display of "shock advised" or "no shock advised" messages, and therapy delivery remains available. Additionally, this nonconformance is limited to the device on-screen prompts only; rhythm analysis is not impacted by this issue.
Official recall notice
LIFEPAK ® 35 Monitor/Defibrillator
Agency: Health Canada
Official publication date: September 2, 2026
Read the official CANADA_HEALTH recall notice →SCAN ONCE. KEEP WATCHING.
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