FDA recall record

Bairn Biologics Candisol recall — FDA F-0163-2014

Firm was notified by supplier of xylanase enzymes that they were contaminated with Chloramphenicol.

Class IIclassification
F-0163-2014official record ID
Nov 20, 2013report date

Recall record at a glance

Official recordF-0163-2014
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmBairn Biologics
Report dateNov 20, 2013
Recall initiation dateOct 24, 2013
Quantity8232 bottles of 40 count; 27, 882 bottles of 120 count.
LocationLas Vegas, NV, United States

Official product description

Bairn Biologics Candisol; Natural Enzymes to Support a Health Gastrointestinal Tract. Dietary Supplement; Ingredients: Vegetarian Cellulase, Vegetarian Hemicellulase, Vegetarian Xylanase, Vegetarian Beta-glucanase, microcrystalline Cellulose, L-Leucine, Vegetable Capsule. Packaged in 40 and 120 count amber glass bottles. Bairn Biologics, P.O. Box 95966 Las Vegas, NV 89183

Why the product was recalled

Firm was notified by supplier of xylanase enzymes that they were contaminated with Chloramphenicol.

Distribution information

US and Australia, Guatemala, United Kingdom, Israel, Canada and Japan.

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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