Pro-pak Custom Pack For Cataract And Specialty Ophthalmic Procedures

Recall Summary Pro-Pak Custom Pack for Cataract and Specialty Ophthalmic Procedures is being recalled across Canada due to a medical device issue. This product is used by healthcare facilities during eye surgery procedures. The recall is classified as Class I, which is the most serious type.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-05-31

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/4e318e5c-d67e-4fa0-ba0f-a2a1e45b782f