United StatesHemochron Activated Clotting Time Low-Range Test Cuvette (REF: ACT-LR), lot E5JLR132, UDI-DI 10711234103081, exp. 08-31-2026, used with the Hemochron Signature ELITE Whole Blood Microcoagulation System is affected. The cuvettes may contain a foreign object with sharp edges that could cause injury if not detected before handling.
What's being recalled
Hemochron Activated Clotting Time Low-Range Test Cuvette, REF: ACT-LR, to be used with the Hemochron Signature ELITE Whole Blood Microcoagulation System
Recalling firm: Accriva Diagnostics, Inc., San Diego, CA, United States.
How to identify it
UDI-DI: 10711234103081. Lot: E5JLR132. Expiration: 08-31-2026
The hazard
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.
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
Worldwide - US Nationwide distribution including in the states of OH, IL, NY, GA, CA, IN, NJ, TX, KS, NE, FL, SC, MO, WV, WA, MI, CO, TN, PA, UT, LA, MT, NC, KY, TX and the countries of CA.
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)
Canada