Pristina Serena (senoaxys) (2019-05-19)

Pristina Serena Recall Summary Pristina Serena, a medical device distributed across Canada, has been recalled due to safety or effectiveness concerns. The device was classified as a Class I recall, which is the most serious type. This recall affects all units of the product that were distributed in Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2019-05-31

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/fe39a3a3-1eb5-4636-9853-3805ff86df94