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Remel Yeastone Broth
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MEDICAL DEVICE RECALLMODERATE

Remel Yeastone Broth

Remel is recalling Yeastone Broth due to the potential for incorrect antimicrobial susceptibility testing results.

What to do

Laboratory personnel should immediately discontinue use of the affected product and follow the manufacturer's instructions for returning or disposing of the inventory.

Recalled
Listed
Updated
Recall No.
Z-1806-2026
Agency
FDA
Firm
Remel, Inc
Recall ID
98616
Status
ONGOING

Why it was recalled

Remel is recalling Yeastone Broth due to the potential for incorrect antimicrobial susceptibility testing (AST) results during quality control. This issue may lead to delayed treatment or the need for alternative antifungal therapy if laboratory quality control results are ignored.

Is mine affected?

Check the model, lot, or serial number on the device or its packaging. Yours is affected if it matches one below.

Yeastone Broth, 11ML, 10/BOX YY3462

UDI-DI
848838018817

Where it was sold

Distributed nationwide.

Timeline

  1. Firm initiated recall
  2. Publicly announced
  3. Listed on Recall Canary
  4. Summary updated

Official source

View on U.S. Food and Drug Administration →

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Editorial summary by Recall Canary · summary updated 2026-06-11 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification