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FDA recall record

Dietary Supplement packaged in the following configuration: (1)Nutri-Essence Digestion Super Potency Enzymes & Herbs with patent-pending CereCalase Plus, packaged in 180-(SKU...

Recall F-0735-2014Class 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 Supplement packaged in the following configuration: (1)Nutri-Essence Digestion Super Potency Enzymes & Herbs with patent-pending CereCalase Plus, packaged in 180-(SKU 51832) capsule bottles. , Parkville, MO (2) Positive Changes Hypnosis Centers Enzymes Digestion Dietary Supplement packaged in 60-(SKU 53793) and 180-(SKU 53794) capsule bottles.

The firm name on the bottle is Positive Changes Hypnosis Center Dublin, OH 43017

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 Supplement packaged in the following configuration: (1)Nutri-Essence Digestion Super Potency Enzymes & Herbs with patent-pending CereCalase Plus, packaged in 180-(SKU 51832) capsule bottles. , Parkville, MO (2) Positive Changes Hypnosis Centers Enzymes Digestion Dietary Supplement packaged in 60-(SKU 53793) and 180-(SKU 53794) capsule bottles.

    The firm name on the bottle is Positive Changes Hypnosis Center Dublin, OH 43017

Code information listed by FDA

Lot Numbers: 51832027, 53793001, 53793002, 53794001, and 54426000

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: 1,587 bottles

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.