Accriva Diagnostics recalls

Accriva Diagnostics appears in 7 official U.S. recall notices indexed by RecallRadar, most recently on 2026-06-24.

Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.

• directCHECK ACT-LR whole blood quality control, level 2 Model/Catalog Number: DCGLR-2
  FDA Device · Class II · 2026-06-24 · Accriva Diagnostics
• Hemochron Activated Clotting Time Low-Range Test Cuvette, REF: ACT-LR, to be used with the Hemochron Signature ELITE Whole Blood Microcoagu…
  FDA Device · Class II · 2025-12-10 · Accriva Diagnostics
• VerifyNow PRUTest Platelet Reactivity Test REF 85225 UDI-DI code: 10711234150078 The VerifyNow PRUTest is a whole blood test used in the la…
  FDA Device · Class III · 2025-11-19 · Accriva Diagnostics
• VerifyNow P2Y12 Platelet Reactivity Test, REF: 85064
  FDA Device · Class II · 2025-01-22 · Accriva Diagnostics
• AVOXimeter 1000E, Product Number: AVOX1000E. The AVOXimeter 1000E is a battery-operated bedside whole blood oximeter
  FDA Device · Class II · 2024-11-06 · Accriva Diagnostics
• The VerifyNow P2Y12 Test is designed to measure platelet P2Y12 receptor blockade
  FDA Device · Class II · 2022-06-01 · Accriva Diagnostics
• Accriva- APTT Cuvette for use on the Hemochron Jr. test system, catalog #J103, lot B6JCA012
  FDA Device · Class II · 2016-06-01 · Accriva Diagnostics