Official recall record
LIFEPAK ® 35 Monitor/Defibrillator (ref 82590)
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2026-09-02
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
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.
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-09-12.
Record last checked against the registry on 2026-09-12.
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