FDA recall record

Remel Oxoid Legionella BCYE Growth Supplement packaged in packs of 10-100ml vials recall — FDA Z-0578-2015

Use of the product could result in inadequate recovery of Legionella pneumophila which could result in false negative reporting.

Class IIclassification
Z-0578-2015official record ID
Dec 17, 2014report date

Recall record at a glance

Official recordZ-0578-2015
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmRemel Inc.
Report dateDec 17, 2014
Recall initiation dateNov 13, 2014
Quantity1/10/100 ml/vials/packs
LocationLenexa, KS, United States

Official product description

Oxoid Legionella BCYE Growth Supplement packaged in packs of 10-100ml vials. A growth supplement for the isolation of Legionella.

Why the product was recalled

Use of the product could result in inadequate recovery of Legionella pneumophila which could result in false negative reporting.

Distribution information

Nationwide Distribution to FL

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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