United StatesSTA Liatest D‑Di, REF 00515 (UDI‑DI 03607450005158), lot numbers 271382 and 271411, expiration 09/30/2025 (12,740 units) distributed worldwide including the U.S. and Canada is affected. It was recalled because of a potential risk of underestimation of D‑Dimer (D‑Di) levels with those two lots.
What's being recalled
Product: STA Liatest D-Di; REF: 00515;
Recalling firm: Diagnostica Stago, Inc., Parsippany, NJ, United States.
How to identify it
REF: 00515; UDI-DI: 03607450005158; Lot numbers: 271382, 271411; Expiration 09/30/2025;
The hazard
A potential risk of underestimation of D-Dimer (D-Di) levels with the two listed lots.
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 distribution- US Nationwide and the country of Canada.
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)