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🇨🇦 directCHECK™ Whole Blood Control

Recall date: May 14, 2026Country: CACategory: medical_devices
Hazard/Reason: Instances of consistently elevated results were identified when using directCHECK™ Whole Blood Control DCGLR‑2, lot A6DLA001. A process error led to testing the lot on the wrong instrument platform, which resulted in the creation and release of incorrect Quality Control (QC) ranges on the performance range card distributed with this lot.
This page links to official sources. Verify model/lot/batch details in the official notice.