Accriva Diagnostics, Inc. recalls
3 recalls filed under Accriva Diagnostics, Inc.. The most recent was published June 24, 2026.
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Class II · 4 months ago
Accriva Diagnostics, Inc. directCHECK ACT-LR whole blood quality control recall: Assayed Whole blood control contains labeling with incorrect performance range
Assayed Whole blood control contains labeling with incorrect performance range.
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Class II · 11 months ago
Accriva Diagnostics, Inc. Hemochron Activated Clotting Time Low-Range Test Cuvette recall: Test cuvettes, used with an assay for monitoring heparin anticoagulation
Test cuvettes, used with an assay for monitoring heparin anticoagulation, may have a foreign object that has sharp edges and could pose a risk of…
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Class III · 11 months ago
Accriva Diagnostics, Inc. VerifyNow Prutest Platelet Reactivity Test REF 85225 Udi-Di recall: Due to an device without a premarket clearance being incorrectly package
Due to an device without a premarket clearance being incorrectly package and distributed.
About this page
Accriva Diagnostics, Inc. appears here because a federal agency named it as the recalling firm or the brand on the label. A recall is not a judgement about everything the company sells — it covers only the lot codes and models listed in each notice.