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Accriva Diagnostics, Inc.

Accriva Diagnostics, Inc.: 2 recalls posted by FDA since June 2026.

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All recalls (2)

Accriva Diagnostics Hemochron Jr. APTT Test Cuvettes

The Hemochron Jr. APTT test cuvette may have a mispositioned or absent reagent, causing erroneous results and potential thrombosis.

Moderate risk, FDA, , Device defect

DirectCHECK ACT-LR Whole Blood Quality Control, Level 2

The directCHECK ACT-LR whole blood quality control has labeling with an incorrect performance range.

Moderate risk, FDA, , Labeling error
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