Class IITerminated in FDA datasetOct 30, 2013

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…

Recalling firm: National Enzyme Co

Why it was recalled

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

Check the codes ↓

The exact product

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. The firm name on the label is Enzymes, Inc., 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

Check the codes

Compare these FDA-provided codes, lot numbers or dates with the product you have.

Match the product, size and code together. A similar name alone does not identify your batch.

Original FDA code information

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

Recall details

Recall number
F-0735-2014
Event ID
66658
FDA status
Terminated
Initiated
Oct 30, 2013
Reported
Dec 25, 2013
Classified
Dec 13, 2013
Terminated
Mar 3, 2015
Quantity
1,587 bottles
Location
Forsyth, MO, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

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.

FDA source record · F-0735-2014

Data updated September 16, 2026. View official FDA data ↗

A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.