Medical device recalls Moderate risk

Strep Selective II Agar recalled over Listeria risk

Recall date
July 11, 2025
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Official notice title
Remel, Inc recalls Strep Selective II Agar, Product Number R01859
Recall number
Z-2224-2025
FDA classification
Class II
Brand / firm
Remel, Inc
Sold / distributed
US Nationwide distribution.

Why it was recalled

The products may contain surface and subsurface contamination of Listeria monocytogenes.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Strep Selective II Agar, Product Number R01859

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