Dimension Vista System-prealbumin Assay

Recall Summary The Dimension Vista System-Prealbumin Assay, a medical device used to measure prealbumin levels in blood samples, is being recalled across Canada. The recall is classified as Class I, which indicates a serious issue with the device. The specific reason for the recall relates to problems with the medical device itself.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2017-02-27
Status
Closed
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/a87810ce-ba8e-4a0a-98ad-3ce118856ed9