Emit® 2000 Quinidine Assay

Recall Summary Siemens Healthcare Diagnostics Inc. is recalling the EMIT® 2000 Quinidine Assay across Canada due to a device performance issue. This assay is a laboratory test used to measure quinidine levels in patient blood samples. The recall is classified as Class II, meaning the device could potentially cause adverse health consequences or serious adverse health consequences.

Product

EMIT® 2000 Quinidine Assay

Reason

Device performance issue

Classification

Class II

Category

medical device recall

Country

Canada

Agency

HC-DEVICES

Recall date

2026-10-15

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/7efa1211-da72-45d9-a869-15678d476e68