FDAClass IIMarch 11, 2015

Oxoid Legionella BCYE Growth Supplement SR0110A recall

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.

Why was Oxoid Legionella BCYE Growth Supplement SR0110A recalled?

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

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Lot No. 1545171

Product
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.
Recalling firm
Remel Inc
Quantity
24 packs (10 x 100 ml vials)
Distribution
US Distribution to the states of : MI, ND, SC, TN, and TX.
Recall date
March 11, 2015
Classification
Class II
Status
Terminated
Agency
FDA (device)
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