Hologic Myosure Rod Lens Hysteroscope (2017-12-11)

Hologic MyoSure Rod Lens Hysteroscope Recall Hologic is recalling MyoSure Rod Lens Hysteroscopes used in Canada due to a defect in the optical lens component. The devices were distributed across Canada and used in medical procedures. This is a Class I recall, which indicates a serious issue with the device.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-12-21

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/e5f5e12b-439a-421c-856a-78afc40c02f9