United StatesZYMUTEST HIA IgG in vitro diagnostic ELISA kit (Ref. RK040A), Lot FD1265, UDI-DI 03663537018763, packaged on 17 October 2024 and distributed in CA, GA, MN, MO, NC, NM, NY, VA, WA, and WI, is affected. Aniara Diagnostica LLC recalled these kits because they were packaged with an outdated flyer dated 8 October 2024 that contains incorrect values for the positive control.
What's being recalled
ZYMUTEST HIA IgG, in vitro diagnostic ELISA kit, Ref. RK040A
Recalling firm: Aniara Diagnostica LLC, West Chester, OH, United States.
How to identify it
UDI-DI: 03663537018763; Lot Number: FD1265
The hazard
Kits from lot FD1265 had been packaged on 17 October 2024 and put on the market with an outdated flyer (8 October 2024), containing incorrect values for the positive control.
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
US Nationwide distribution in the states of CA, GA, MN, MO, NC, NM, NY, VA, WA, and WI
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)