Official recall record
Heartsine Samaritan PAD 360P, 500P, and 350P
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2024-04-04
- Last updated (per notice)
- 2025-01-14
- Country of alert
- Canada
- Alert level
- Type I
- Alert type
- recall
What the authority reported
Stryker has determined that a manufacturing related issue may impair device audio prompts. Stryker is issuing a customer notification to remind customers to follow the user manual and power the device upon receipt to ensure the audio prompts function as intended. Recall Start Dates: March 21, 2024
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 2026-05-31.
Record last checked against the registry on 2026-05-31.
ProductGuru Recalls republishes official safety information with attribution. We are not
the issuing authority and this page is not advice. If this product is a medical device or
medication, speak to a doctor or pharmacist. Found an error?
Report it — corrections are published.