St Aia-pack Ft3 (2018-12-04)

Recall Summary ST AIA-PACK FT3 medical devices have been recalled across Canada due to safety concerns. The recall is classified as Class I, indicating a serious issue with the device. This recall affects consumers who have this device in Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2019-01-08

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/24bc00d0-5f7c-4d5d-8201-4111b9f46b8e