Product Wiki · Recalls · Health Canada — Medical Devices

Cardiohelp-i — recall 74679

Health Canada — Medical Devices · Canada · 2023-12-04 · 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: 74679
Date of alert: 2023-12-04
Country / jurisdiction: Canada
Risk level: Type II
Risk type: recall
Product category: Gastroenterology and urology
Product type: Medical devices

Reported risk: The quality issue under investigation is applicable to the "connection cable venous probe, l0.23m". The part causing the nonconformance under investigation is responsible for data transmission between the Cardiohelp-i and the venous probe. A noticeable high number of breaks in the insulation sheath and a shielding breach of the venous probe connection cable was observed. Recall Start Date: November 21, 2023

Primary source: https://recalls-rappels.canada.ca/en/alert-recall/cardiohelp-2

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.

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.

Cardiohelp-i — recall 74679

Related