Mmonia L3k Assay

Ammonia L3K Assay Recall Summary The Ammonia L3K Assay, a medical device used for testing, is being recalled across Canada due to safety or performance concerns. This is a Class I recall, which means the product poses a serious risk to health. The recall affects all Canadian customers who have this device.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2016-12-13
Status
Closed
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/28333d5a-0ef4-49a3-828f-223a88f6984d