Medical device recalls Moderate risk

Remel Inc recalls Oxoid Legionella BCYE Growth Supplement SR0110A packaged in packs of 10- 100 ml vials. The responsible firm name on the…

Recall date
February 5, 2015
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1232-2015
FDA classification
Class II
Brand / firm
Remel Inc
Sold / distributed
US Distribution to the states of : MI, ND, SC, TN, and TX.

Why it was recalled

Use of the product may not provide adequate recovery and could result in false negative identification of Legionella pneumophila.

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

What was recalled

Oxoid Legionella BCYE Growth Supplement SR0110A packaged in packs of 10- 100 ml vials. The responsible firm name on the label is Oxoid Ltd., Basingstoke, Hampshire, England and Oxoid Ltd., Basingstoke, Hants, England.

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