Dimension Vista System-lactate Dehydrogenase Flex (ldi) Assay (2018-10-17)

Recall Summary The Dimension Vista System-Lactate Dehydrogenase Flex (LDI) Assay has been recalled across Canada due to issues with the medical device. This is a laboratory test used to measure lactate dehydrogenase levels in blood samples. The recall affects healthcare facilities and laboratories that use this assay system.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2018-11-02

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/0728e827-b7a3-496e-81fe-38b2d553b8de