Product Wiki · Recalls · Health Canada — Medical Devices

Med-Rx Epidural Anesthesia Kit — recall 64394

Health Canada — Medical Devices · Canada · 2022-07-25 · 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
64394
Date of alert
2022-07-25
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Anaesthesiology
Product type
Medical devices
Reported risk: This recall addresses an incorrect needle size concern in the kits. Some of the needles for product code 80-8139 and lot 163309 contained shorter sized needles instead of the labelled larger size (3.5 inch). Recall start date: July 14, 2022
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/med-rx-epidural-anesthesia-kit

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.