United StatesHemosIL SynthAFax Partial Thromboplastin Time Tests (Part No. 0020007400; UDI 08426950087649) with Lot Nos. N0542231 (exp. 2026-06-30), N0250088 (exp. 2027-04-30), and N0452249 (exp. 2027-06-30) are being recalled by Instrumentation Laboratory. They were recalled because the recalled lots were manufactured with double the amount of preservative concentration.
What's being recalled
HemosIL SynthAFax. Partial Thromboplastin Time Tests.
Recalling firm: Instrumentation Laboratory, Bedford, MA, United States.
How to identify it
Part No. 0020007400; UDI: 08426950087649; Lot No. (Exp. Date) N0542231(2026-06-30), N0250088(2027-04-30, N0452249 (2027-06-30).
The hazard
Recalled lots were manufactured with double the amount of preservative concentration.
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
Domestic: CA, CO, FL, NY; Foreign: AR, AT, CA, CZ, DE, DK, ES, FR, GB, IE, IL, IN, IT, JP, LK, NL, PL, PT, RO, RS, TH, VN.
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)