Zymutest Hia Iggam (2017-11-09)

Summary ZYMUTEST HIA IGGAM has been recalled across Canada due to a medical device issue and classified as a Class I recall (the most serious category). The recall affects this drug product that was distributed nationwide in Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-11-30

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/b2d5a0a0-5ed9-4ca1-a5c3-1371ed7c388e