Aesculap Unlicenced Medical Devices

Aesculap Unlicensed Medical Devices Recall Aesculap medical devices are being recalled across Canada because they were not authorized by Health Canada before being sold. This is a Class I recall, meaning the devices could cause serious harm or death. The recall affects all Aesculap unlicensed medical devices distributed throughout Canada.

Product

Aesculap unlicenced medical devices

Reason

Unauthorised device

Classification

Class II

Category

medical device recall

Country

Canada

Agency

HC-DEVICES

Recall date

2026-01-15

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/7786a3fd-9fce-4b39-bd8c-e13e3a396e9c