⚠ RecallRadar📷 ScanGuidesOfficial U.S. recall notices, restated plainly

Accriva Diagnostics recalls - full list & free alerts

3 official U.S. recalls involving Accriva Diagnostics in the last 12 months, most recently on 2026-06-24.

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Full list (3)

Accriva Diagnostics, Inc.: directCHECK ACT-LR whole blood quality control, level 2 Model/Catalog Number: DCGLR-2
Medical DevicesFDA (device) · 2026-06-24 · Class II
Accriva Diagnostics, Inc.: Hemochron Activated Clotting Time Low-Range Test Cuvette, REF: ACT-LR, to be used with the Hemochron Signature ELITE Whole Blood Microcoagul
Medical DevicesFDA (device) · 2025-12-10 · Class II
Accriva Diagnostics, Inc.: VerifyNow PRUTest Platelet Reactivity Test REF 85225 UDI-DI code: 10711234150078 The VerifyNow PRUTest is a whole blood test used in the
Medical DevicesFDA (device) · 2025-11-19 · Class III