Medical device recalls Moderate risk

Remel Blood Agar plate REF R01202 packaged 10 plates per pack recalled over Listeria risk

Recall date
May 4, 2015
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Official notice title
Remel Inc recalls Remel Blood Agar (TSA w/sheep blood) plate REF R01202 packaged 10 plates per pack, 10/10-packs per case (100 plates). B…
Recall number
Z-1748-2015
FDA classification
Class II
Brand / firm
Remel Inc
Sold / distributed
Nationwide Distribution.

Why it was recalled

Product may be contaminated with 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

Remel Blood Agar (TSA w/sheep blood) plate REF R01202 packaged 10 plates per pack, 10/10-packs per case (100 plates). Blood agar is a solid medium recommended for use in qualitative procedures for the cultivation of a wide variety of microorganisms and visualization of hemolytic reactions.

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