Dri Salicylate Serum Tox Assay (2016-07-27)

Recall Summary The DRI Salicylate Serum Tox Assay, a medical device used to measure salicylate levels in blood samples, has been recalled across Canada. The recall was issued due to concerns with the device itself, classified as a Class I recall, which indicates a serious issue. This recall affects healthcare facilities and laboratories in Canada that use this testing product.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2016-08-19

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/b1d88c36-84ef-4f9a-bb4f-d48eb13c2c3c