Product Wiki · Recalls · Health Canada — Medical Devices

Medline Disposible Manifolds — recall 81997

Health Canada — Medical Devices · Canada · 2026-04-29 · Type I

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
81997
Date of alert
2026-04-29
Country / jurisdiction
Canada
Risk level
Type I
Risk type
recall
Product category
Cardiovascular
Product type
Medical devices
Reported risk: Specific items and lots of Medline Manifolds are recalled due to presence of particulate within the fluid path of the Manifolds, with the potential to be introduced into blood circulation and become lodged. This carries a risk of serious injury, such as death. Customers have been advised to destroy them.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/medline-disposible-manifolds

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.