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.
Test cuvettes, used with an assay for monitoring heparin anticoagulation, may have a foreign object that has sharp edges and could pose a risk of injury if not detected prior to handling.
Accriva Diagnostics is recalling Hemochron Activated Clotting Time Low-Range Test Cuvettes (REF: ACT-LR) that may have sharp edges. This could cause injury if the cuvette is handled without checking for foreign objects.
The cuvettes may contain a foreign object with sharp edges that can cause injury if not detected before handling. This is a risk during blood sample testing when the cuvette is used with the Hemochron Signature ELITE system.
Users of the Hemochron Signature ELITE blood testing system who own the ACT-LR cuvettes with UDI-DI: 10711234103081 and lot number E5JLR132 are affected. People handling blood samples for heparin monitoring are most at risk.
Check for the UDI-DI number 10711234103081 and lot number E5JLR132 on the cuvette. The cuvette is part of the Hemochron Signature ELITE Whole Blood Microcoagulation System.
Inspect the cuvette for any foreign objects with sharp edges that could cause injury.
Hemochron Activated Clotting Time Low-Range Test Cuvette (REF: ACT-LR) used with the Hemochron Signature ELITE.
The recall is for the specific lot number E5JLR132 with UDI-DI: 10711234103081.
Look for the UDI-DI number 10711234103081 and lot number E5JLR132 on the cuvette.
We’ve drafted a message you can send Accriva Diagnostics to request your refund or repair — edit it as you like.
Subject: Recall Z-0880-2026 — Accriva Diagnostics Accriva Diagnostics Hello, I own a Accriva Diagnostics that is covered by recall Z-0880-2026 from Accriva Diagnostics. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
