Product Wiki · Recalls · Health Canada — Medical Devices

Baxter Flo-Thru, Flo-Rester and Vascular Probe — recall 75204

Health Canada — Medical Devices · Canada · 2024-03-08 · 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
75204
Date of alert
2024-03-08
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Cardiovascular
Product type
Medical devices
Reported risk: Baxter is issuing an important product information letter to communicate that the surgical tools education deck (ref ca-as20-220001) that may have been presented for the products listed, contains inaccurate content that does not align with the products' instructions for use (IFU). Recall start date: February 26, 2024
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/baxter-flo-thru-flo-rester-and

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.