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Medical Device

directCHECK ACT-LR whole blood quality control, level 2 Model/Catalog Number: DCGLR-2

Recall date: 2026-06-24 · Source: FDA_DEVICE
Brand / Firm
Accriva Diagnostics, Inc.
Product
directCHECK ACT-LR whole blood quality control, level 2 Model/Catalog Number: DCGLR-2
Reason for recall
Assayed Whole blood control contains labeling with incorrect performance range.
Units affected
6060
Description
directCHECK ACT-LR whole blood quality control, level 2 Model/Catalog Number: DCGLR-2
View official recall notice →