Cobas Ampliprep/cobas Taqman Hcv Quantitative & Qualitative Test, V2.0 (2019-10-23)

Recall Summary Roche's Cobas AmpliPrep/Cobas TaqMan HCV tests (version 2.0) are being recalled across Canada due to a device defect. These tests are used in laboratories to detect and measure hepatitis C virus in blood samples. The recall affects healthcare facilities and diagnostic laboratories that use this testing system.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2019-12-06
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/66da473a-1fea-4a08-a730-e2b473e45125