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FDA recall record

Dietary Supplements packaged in the following configurations: (1) Heryben, Eumin Integrated Plant Enzymes, packaged 60 capsule bottles(SKU 54440). Firm name on the label is Ac...

Recall F-0799-2014Class IITerminatedOctober 30, 2013

FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.

FDA listed a termination date of March 3, 2015. openFDA does not treat this as a live recall-status tracker.

Product described in an FDA recall

Dietary Supplements packaged in the following configurations: (1) Heryben, Eumin Integrated Plant Enzymes, packaged 60 capsule bottles(SKU 54440).

Firm name on the label is ActiFit Biotechnology, Bellevue, WA; (2) Bulk C269 Shanghai Digestive Blen capsules, packaged in varying quantities within poly bags within corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 92473);

Reason

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

Products involved

Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.

  • Dietary Supplements packaged in the following configurations: (1) Heryben, Eumin Integrated Plant Enzymes, packaged 60 capsule bottles(SKU 54440).

    Firm name on the label is ActiFit Biotechnology, Bellevue, WA; (2) Bulk C269 Shanghai Digestive Blen capsules, packaged in varying quantities within poly bags within corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 92473);

Code information listed by FDA

Lot #: 54440000 and 92473000

Distribution and firm information

Recalling firm listed by FDA: National Enzyme Co

Firm location listed by FDA: Forsyth, MO, United States

Distribution reported by FDA: 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.

Product quantity listed by FDA: 3640 bottles and 210,098 bulk capsules

Source

Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.

Official FDA openFDA food enforcement record

Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.