[Recalled] Aesculap unlicenced medical devices — Unauthorised device | Health Canada 2026-01-15
The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.
Recall details
| Product | Aesculap unlicenced medical devices |
|---|---|
| Category | General and plastic surgery - Gastroenterology and urology - Orthopaedics - Neurology - Ophthalmology - Obstetrics and g |
| Issuing authority | HC |
| Reference | 81485 |
| Country of notice | Canada |
| Risk level | Type II |
| Hazard type | recall |
| Notice date | 15 January 2026 |
Why it was recalled
According to the HC notice, the identified hazard is: Unauthorised device
This Type II recall concerns General and plastic surgery - Gastroenterology and urology - Orthopaedics - Neurology - Ophthalmology - Obstetrics and g 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.