Gglu. Sera Shigella Boydii Polyvalent 2 (7 To 11) (2018-07-03)

Recall Summary Agglu. Sera Shigella boydii polyvalent 2 (7 to 11) diagnostic serum is being recalled across Canada due to issues with the medical device. This product is classified as a Class I recall, which indicates a serious problem. The recall affects this specific laboratory diagnostic serum used for identifying Shigella bacteria.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2018-08-17

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/374fb962-45ee-43a7-8381-2f373d3916e2