Product Wiki · Recalls · Health Canada — Medical Devices

Heartsine Samaritan Pad 500P — recall 72667

Health Canada — Medical Devices · Canada · 2023-02-09 · Type II

Compiled from an official source — the facts on this page are reproduced from the issuing authority’s own published notice, which is linked above. No AI-generated text appears on this page. How we use AI →
Agency
Health Canada — Medical Devices
Recall identifier
72667
Date of alert
2023-02-09
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Cardiovascular
Product type
Medical devices
Reported risk: Stryker has identified that there is a potential that the affected device was shipped with the incorrect language configuration. Recall start date: January 26, 2023
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/heartsine-samaritan-pad-500p

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

Related

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.