Product Wiki · Recalls · Health Canada — Medical Devices

3-D Matrix Syringe Adapter — recall 73808

Health Canada — Medical Devices · Canada · 2023-06-13 · 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
73808
Date of alert
2023-06-13
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
General hospital and personal use
Product type
Medical devices
Reported risk: The device 3-D Matrix Syringe Adapter does not meet the requirements of the medical device regulations. (Not licensed for use in Canada). There is no adapter defect. The 3-D Matrix Syringe Adapter it is an optional accessory for Purastat. Purastat is a licensed class IV device in Canada. Recall start date: May 17, 2023
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/3-matrix-syringe-adapter

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.