Every recall we track for Accriva Diagnostics, Inc. — 6 in all — plus the complaints and injury reports the public filed about them.
Accriva Diagnostics recalls directCHECK ACT-LR whole blood quality control level 2 (DCGLR-2) due to incorrect performance range labeling on the control kit.
Accriva Diagnostics recalls Hemochron Activated Clotting Time Low-Range Test Cuvettes (REF: ACT-LR) used with Hemochron Signature ELITE. Sharp edges may cause injury if not detected before handling.
Accriva Diagnostics recalls VerifyNow PRUTest Platelet Reactivity Test REF 85225 with UDI-DI code 10711234150078 due to being distributed without premarket clearance. This may pose risks in laboratory or point-of-care testing.
a ~150-character meta description summarising the recall.
Accriva recalls AVOXimeter 1000E bedside blood oxygen monitors that may show falsely high oxygen levels, risking incorrect patient care. Affected units have specific product numbers and serial numbers.
a ~150-character meta description summarising the recall.
