FDA Device recall Z-1806-2026
Yeastone Broth, 11ML, 10/BOX YY3462
- FDA Device
- Class II
- ongoing
- Published 2026-04-22
On 2026-04-22 the FDA classified a Class II recall of Yeastone Broth, 11ML, 10/BOX YY3462 by Remel, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1806-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-03-24 |
| Published | 2026-04-22 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Remel |
| Distribution | US |
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.
Identifiers
| code_info | UDI-DI 848838018817 lots 321046, 329835, 330316, 327069, 330317, 336325, 338314, 341161, 303851, 311723 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1806-2026%22
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