Remel, Inc recalls Yeastone Broth
- Recalling company
- Remel, Inc
- Product
- Yeastone Broth, 11ML, 10/BOX YY3462
- Reason
- 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.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Mar 24, 2026
- Reported
- Apr 22, 2026
- Distribution
- Worldwide distribution - US Nationwide and the countries of Canada, Vietnam, France, Argentina, Qatar, New Zealand, Uruguay, Turkey, Netherlands, Singapore.
- Status
- Ongoing
- Quantity
- 2819
- Lot / codes
- UDI-DI 848838018817 lots 321046, 329835, 330316, 327069, 330317, 336325, 338314, 341161, 303851, 311723
- Company location
- Lenexa, KS
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-1806-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-1806-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.