Quanta Lite Histone Elisa (2019-12-20)

QUANTA Lite Histone ELISA Recall Summary The QUANTA Lite Histone ELISA, a medical test kit used to detect histones in patient samples, is being recalled across Canada due to quality or safety issues with the device. This recall is classified as Class I, meaning there is a serious potential for harm. The product was distributed nationwide in Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2020-01-10
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/b09fd061-a4d0-4782-8d3d-07012a473bc0