United StatesYeastone Broth, 11 mL, 10/box (YY3462), UDI‑DI 848838018817, lots 321046, 329835, 330316, 327069, 330317, 336325, 338314, 341161, 303851 and 311723 is affected. The product was recalled because it may report incorrect antimicrobial susceptibility testing (AST) results during quality control, which could lead to a delayed response or the need to change to another antifungal agent if a laboratory ignores the quality control test result.
What's being recalled
Yeastone Broth, 11ML, 10/BOX YY3462
Recalling firm: Remel, Inc, Lenexa, KS, United States.
How to identify it
UDI-DI 848838018817 lots 321046, 329835, 330316, 327069, 330317, 336325, 338314, 341161, 303851, 311723
The hazard
Products may report incorrect AST results during quality control. Health consequences may include delayed response or the need to change to another antifungal agent if laboratory ignores Quality Control test result.
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 countries of Canada, Vietnam, France, Argentina, Qatar, New Zealand, Uruguay, Turkey, Netherlands, Singapore.
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)