FDA recall record

National Enzyme Co Houston Enzymes TriEnza with DPP IV Activity, Broad-Spectrum recall — FDA F-0734-2014

Firm is recalling dietary supplements containing a raw material which may contain >0.3 ppb chloramphenicol

Class IIclassification
F-0734-2014official record ID
Dec 25, 2013report date

Recall record at a glance

Official recordF-0734-2014
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmNational Enzyme Co
Report dateDec 25, 2013
Recall initiation dateOct 30, 2013
Quantity54,887 bottles, and 327,139 bulk capsules
LocationForsyth, MO, United States

Official product description

Houston Enzymes TriEnza with DPP IV Activity, Broad-Spectrum Enzyme Product for general Digestive Support, packaged in 90-(SKU 53379) and 180-(SKU 53380) capsule bottles. The firm name on the label is Houston Nutraceuticals, Inc. (HNI), Siloam Springs, AR (2) 9212 TRIENZA Bulk Capsules (SKU 91980) packaged in varying quantities in poly bags within corrugated containers.

Why the product was recalled

Firm is recalling dietary supplements containing a raw material which may contain >0.3 ppb chloramphenicol

Distribution information

Domestic distribution of the product is nationwide with direct accounts in 27 states in all geographical regions. Foreign distribution consists of direct accounts in the following countries: Canada, China, Malaysia, Norway, Slovakia, South Korea, Sweden, Taiwan, and the United Kingdom.

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: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

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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