Product Wiki · Recalls · Health Canada — Medical Devices

Cardinal Health Monoject™ syringes — recall 74925

Health Canada — Medical Devices · Canada · 2024-01-18 · 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
74925
Date of alert
2024-01-18
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
General hospital and personal use
Product type
Medical devices
Reported risk: Medical device labeling correction to inform customers that Cardinal Health branded Monoject™ syringes have not been validated for use with the Caesarea Medical Electronics (CME) devices. Recall start date: November 8, 2023
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/cardinal-health-monojecttm-syr

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.