Intercept I2 Oral Fluid (2016-04-13)

Intercept I2 Oral Fluid Recall Summary The Intercept I2 Oral Fluid drug testing device is being recalled across Canada due to issues with the medical device itself. This Class I recall affects all units of this product that were distributed throughout Canada. The recall was initiated on April 13, 2016.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2016-04-29
Status
Closed
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/7c39536b-5575-4177-9bb6-66c9e67548e4