FDA
Food and Drug Administration · Recall Z-2460-2026 · Apr 30, 2026directCHECK ACT-LR whole blood quality control, level 2 Model/Catalog Number: DCGLR-2
Accriva Diagnostics, Inc.
The hazard
Assayed Whole blood control contains labeling with incorrect performance range. FDA Class II recall.
The remedy
Follow FDA guidance
About this recall
directCHECK ACT-LR whole blood quality control, level 2 Model/Catalog Number: DCGLR-2
Affected identifiers
Check these against the label on your unit. An identifier match is how a recall is confirmed, not just suspected.
Model Lot #: A6DLA001 Unique Device Identifier: 10711234170373UPC 10711234170373Would you have heard about this one?
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Start monitoring freeSourced from the Food and Drug Administration’s public recall data. Always verify serial and date ranges against the official notice before acting.