RecalledThisWeek Search
Medium risk Medical DevicesClass II

Remel Yeastone Broth Recall

Yeastone Broth, 11ML, 10/BOX YY3462

Updated March 24, 2026

Remel Yeastone Broth test kits may give incorrect results during quality control checks, potentially delaying treatment decisions for fungal infections. Laboratories relying on faulty quality control results could miss the need to switch antifungal medications.

Is the Remel, Inc recalled? Yes. This product was recalled by FDA on March 24, 2026. Details below.

What is recalled

Yeastone Broth, 11 mL vials, 10 per box, lot YY3462, manufactured by Remel, Inc.

Am I affected

You're affected if your laboratory uses Yeastone Broth lot YY3462 for antifungal susceptibility testing or quality control checks.

What to do right now

If you operate or work in a laboratory using this product, stop relying on quality control results from lot YY3462 and contact Remel, Inc. directly for guidance on replacement or verification of prior test results.

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.

Brands affected

Remel, Inc
Source
FDA
Category
Medical Devices
Recall ID
fda-Z-1806-2026
Classification
Class II
Recalled
March 24, 2026
Read the official notice

Get free recall alerts

New Medical Devices recalls, the moment they post.

Free forever. Unsubscribe anytime. We never sell your data.

More Medical Devices recalls