OFFICIAL-SOURCE RECALL · CANADA
LIFEPAK ® 35 Monitor/Defibrillator Recall: During production of LP35, Stryker identified that
Use the identifiers printed on your item to determine whether this recall may affect the product you own.
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Is your product affected?
- Brand
- See official notice
- Product
- LIFEPAK ® 35 Monitor/Defibrillator
- Manufacturer
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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
During production of LP35, Stryker identified that certain printer and modem access port connectors may not have been fully seated within the rear housing assembly. As a result, the connectors may appear flush with or recessed relative to the retaining nut rather than extending beyond it as intended.
Hazard
During production of LP35, Stryker identified that certain printer and modem access port connectors may not have been fully seated within the rear housing assembly. As a result, the connectors may appear flush with or recessed relative to the retaining nut rather than extending beyond it as intended.
Official recall notice
LIFEPAK ® 35 Monitor/Defibrillator
Agency: Health Canada
Official publication date: September 4, 2026
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