Iol Master 700 (2015-02-04)

IOL Master 700 Recall Summary The IOL Master 700 device has been recalled across Canada due to a health products issue. This device is used in medical settings to measure the eye for cataract surgery planning. The recall is classified as Class I, which is the most serious type of recall classification.

Reason

Health products

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2016-07-22

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/029d0ce3-569b-4466-b41e-eb2ad36174db