PlainRecalls
FDA Food Moderate Class II Terminated

Dietary Supplements packaged in the following configurations: (1) Bulk B341 Shanghai Actizyme Tab6 tablets, packaged in varying quantities within poly bags within corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 92275); (2) ActiFIT, Actizyme, Digest Miracle, packaged in 60-tablet bottles (SKU 54955). Firm name on the label is ActiFit Biotechnology Co, Bellevue, WA.

Reported: December 25, 2013 Initiated: October 30, 2013 #F-0787-2014

Product Description

Dietary Supplements packaged in the following configurations: (1) Bulk B341 Shanghai Actizyme Tab6 tablets, packaged in varying quantities within poly bags within corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 92275); (2) ActiFIT, Actizyme, Digest Miracle, packaged in 60-tablet bottles (SKU 54955). Firm name on the label is ActiFit Biotechnology Co, Bellevue, WA.

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
321,893 bulk capsules, 3714 bottles.
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?
Dietary Supplements packaged in the following configurations: (1) Bulk B341 Shanghai Actizyme Tab6 tablets, packaged in varying quantities within poly bags within corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 92275); (2) ActiFIT, Actizyme, Digest Miracle, packaged in 60-tablet bottles (SKU 54955). Firm name on the label is ActiFit Biotechnology Co, Bellevue, WA.. Recalled by National Enzyme Co. Units affected: 321,893 bulk capsules, 3714 bottles..
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-0787-2014.