PlainRecalls
FDA Food Moderate Class II Terminated

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.

Reported: December 25, 2013 Initiated: October 30, 2013 #F-0734-2014

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.

Reason for Recall

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

Details

Recalling Firm
National Enzyme Co
Units Affected
54,887 bottles, and 327,139 bulk capsules
Distribution
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.
Location
Forsyth, MO

Frequently Asked Questions

What product was recalled?
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.. Recalled by National Enzyme Co. Units affected: 54,887 bottles, and 327,139 bulk capsules.
Why was this product recalled?
Firm is recalling dietary supplements containing a raw material which may contain >0.3 ppb chloramphenicol
Which agency issued this recall?
This recall was issued by the FDA Food on December 25, 2013. Severity: Moderate. Recall number: F-0734-2014.