Pneumococci Factor 7f Antisera (2018-11-19)

Pneumococci Factor 7F Antisera Recall Summary Pneumococci Factor 7F Antisera, a medical device used in laboratory testing, was recalled across Canada in November 2018 due to a Class I safety issue. The recall affected all distributed units of this product. No additional details about the specific defect or affected lot numbers are provided in this notice.

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/6e27d2da-5e16-4116-965c-0459f15e48e1