Accriva Diagnostics, Inc.: Medical Device Recalls in 2025

According to to data from the FDA, there were 3 medical device recalls made by Accriva Diagnostics, Inc. in 2025. See the details of the recalls below.

You can see similar recalls for other firms.

• Hemochron Activated Clotting Time Low-Range Test Cuvette, REF: ACT-LR, to be used with the Hemochron Signature ELITE Whole Blood Microcoagulation System
• VerifyNow P2Y12 Platelet Reactivity Test, REF: 85064
• VerifyNow PRUTest Platelet Reactivity Test REF 85225 UDI-DI code: 10711234150078 The VerifyNow PRUTest is a whole blood test used in the laboratory or point of care setting to measure the level of platelet P2Y12 receptor blockade.