# FDA recall F-0739-2014

> **National Enzyme Co** · Class II · food recall initiated 2013-10-30.

## Product

Dietary Supplements packaged in the following configurations:   (1)Transformation Professional Protocol Digest Enzyme Supplement, Packaged in 45-(SKU 54646), 60-(SKU 52413), 90-(SKU 52520), 120-(SKU 53098) capsule bottles. The firm name on the label is Transformation Enzyme Corp. Houston, TX;  (2) 3989V TEC-TPP DIGEST UNL 60' unlabeled 60-(SKU 53571) capsule bottles;  (3) Transformation Digest. Packaged in 60-(SKU 54599) capsule bottles. Russian label;  (4) Anti-aging Nutrition Health Graph Professional Strength Digest Enzyme Supplement. Packaged in 120-(SKU 54752) bottles. The firm name on the label is Health Graph, Glenview, IL;  (5) The Lohad Center for Anti-Aging Digest Enzyme Supplement. Packaged in 90-(SKU 54914) capsules bottles. The firm name on the label is The Lohad Center, Jacksonville, FL.  (6) Bulk 3989V TPP-TEC Digest Conv Pa capsules (SKU 92494) packaged in varying quantities within poly bags within corrugated boxes (for domestic distribution) or fiber drums (for interna

## Reason for recall

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

## 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.

## Key facts

- **Recall number:** F-0739-2014
- **Recalling firm:** National Enzyme Co
- **Classification:** Class II
- **Product type:** food
- **Status:** Terminated
- **Initiation date:** 2013-10-30
- **Report date:** 2013-12-25
- **Termination date:** 2015-03-03

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Forsyth, MO, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=F-0739-2014

## Citation

> AI Analytics. FDA recall F-0739-2014. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/F-0739-2014. Source: US FDA. Licensed CC0.

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