Drugs Of Abuse Cutoff 200% (2019-07-22)

Recall Summary The FDA is recalling Drugs of Abuse Cutoff 200% testing devices distributed across Canada because they are classified as medical devices requiring proper regulatory approval. This recall affects all units of this product that were distributed nationwide in Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2019-08-16

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/7f951363-c55d-4ef6-a79e-acbae8c75730