[Recalled] 3-D Matrix Syringe Adapter — Unauthorised device | Health Canada 2023-06-13

Regulators flagged this product in an official safety action. Here is what the notice says and what it means for owners.

Recall details

Why it was recalled

According to the HC notice, the identified hazard is: Unauthorised device

This Type II recall concerns General hospital and personal use products distributed in Canada and was recorded by HC. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.

What to do if you own this product

Review the official notice to confirm whether your unit is affected.

Read the full official notice →

This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.