Pentacam® Axl Wave And Myopia Master®

Recall Summary Pentacam AXL Wave and Myopia Master devices are being recalled in Canada due to a performance issue. These are medical devices used for eye measurements and analysis. The recall affects all units of these products distributed across Canada.

Product

Pentacam® AXL Wave and Myopia Master®

Reason

Performance

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2023-08-24

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/52c982b8-aebd-41d4-93fb-1dd462dff70e