ACCRIVA DIAGNOSTICS
VERIFYNOW · General Hospital
Recalls (3)
Due to an device without a premarket clearance being incorrectly package and distributed.
Platelet Reactivity Test distributed without appropriate US-FDA market clearance; if used healthcare personnel could use the baseline PRUTest measurement prior to initiating drug therapy, and then use the percent inhibition formula in the notice to manually calculate the percentage of platelet aggregation inhibition for a given patient receiving drug treatment with P2Y12 receptor inhibitor.
Two whole blood Platelet Reactivity tests exist that share the same reagent formulation and are used to obtain P2Y12 Reactivity Unit results. The test without US-FDA market clearance was distributed and it displays BASE results not displayed by the US-FDA market cleared device. A formula is being provided to health care personnel to calculate the percentage of platelet aggregation inhibition.
UDI Registrations (16)
VerifyNow Aspirin Test 25/box
VerifyNow System Electronic Quality Control Device
VerifyNow Printer Kit
VerifyNow System Preventative Maintenance Kit
VerifyNow PRUTest 25/box
VerifyNow System
VerifyNow System (Loaner)
VerifyNow WQC 6/box
VerifyNow System (Refurbished)
VerifyNow System (Loaner)
VerifyNow Aspirin Test 10/box
VerifyNow System (Demonstration)
VerifyNow IIb/IIIa Test 10/box
VerifyNow System Validation Kit
VerifyNow System (Serviced)
VerifyNow System (Demonstration)
FDA Classification (66)
General Hospital
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