Yeastone Broth recall (Remel, Inc)
Medical deviceClass IIOngoing
Summary: Remel, Inc is recalling 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.
What is being recalled
Yeastone Broth, 11ML, 10/BOX YY3462
Why
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.
How serious is it
Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
Where it was sold
Worldwide distribution - US Nationwide and the countries of Canada, Vietnam, France, Argentina, Qatar, New Zealand, Uruguay, Turkey, Netherlands, Singapore.
How to tell if yours is affected
UDI-DI 848838018817 lots 321046, 329835, 330316, 327069, 330317, 336325, 338314, 341161, 303851, 311723
What to do
Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.
Recall facts
| Recall number | Z-1806-2026 |
| Category | Medical device |
| Agency | U.S. Food and Drug Administration (FDA) |
| Severity | Class II |
| Status | Ongoing |
| Recall started | March 24, 2026 |
| Reported | April 22, 2026 |
| Company | Remel, Inc |
| Company location | Lenexa, KS, United States |
| Initiated by | Voluntary: Firm initiated |
| Quantity | 2819 |
More recalls from Remel, Inc · all medical device recalls · recalls from March 2026