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Health Canada Medical devices

Vivos Guides

Issued August 7, 2025
Issue
This recall submission is due to a difference in classification of 1 types of devices; both were originally inputted as Class 1 but after an audit review, the devices are determined to be Class 2 through the audit inspection, and therefore the manufacturer is stopping sale of these device, the Vivos Guides and the Vivos Pex. Recall start date: June 9, 2025
Hazard description
Unauthorised device
Product
Product name
Vivos Guides
Reference
ID
RA-77812