Nti Human Anti Hemophilus Influenza Eia Kit (2019-07-26)

Recall Summary Health Canada has recalled the Anti Human Anti Hemophilus Influenza EIA Kit across Canada due to a medical device issue. This kit is used for laboratory testing to detect antibodies related to Hemophilus influenza infection. The recall is classified as Class I, meaning there is a serious risk associated with the product.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2019-08-23

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/0a2b420f-7d01-427f-8278-a36cb2c18249