Lithium Assay System (2019-07-16)

Lithium Assay System Recall Summary A Lithium Assay System used to measure lithium levels in patient blood samples has been recalled across Canada due to issues with the medical device. This recall affects healthcare facilities and laboratories that use this system for patient testing. The recall is classified as Class I, which indicates a serious potential health concern.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2019-07-26

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/2e57760c-81b5-41c6-adec-604119790674