Severity
Moderate
ModerateClass IITerminated
FDA Food recall · Reported December 25, 2013
Dietary Supplements packaged in the following configurations: (1) Houston Enzymes, No-Fenol, Multi-Enzyme Product for Digestion of Phenolic Foods and Fiber packaged in 90-capsule bottles (SKU 52437). Firm name on the label is Houston Nutraceuticals, Inc. (HNI), Siloam, AR; (2) 5327 Houston NO-FENOL blk 1v, Bulk Capsules (SKU 91456)
Firm is recalling dietary supplements containing a raw material which may contain >0.3 ppb chloramphenicol
Compiled from official public sources by the editorial team.
Verify with FDA Food →
National Enzyme Co recalled Dietary Supplements packaged in the following configurations: (1) Houston Enzymes, No-F… - a moderate-severity action.
Dietary Supplements packaged in the following configurations: (1) Houston Enzymes, No-F… was recalled by National Enzyme Co in December 25, 2013. Reason: Firm is recalling dietary supplements containing a raw material which may contain >0.3 ppb chloramphenicol. Check the official notice for the remedy. Verify recall #F-0745-2014 with the FDA Food before acting.
The recall
National Enzyme Co issued this moderate-severity FDA Food recall — Firm is recalling dietary supplements containing a raw material which may contain >0.3 ppb chloramphenicol.
- Moderate
- severity level
- Class II
- classification
- December 25, 2013
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-0745-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-0745-2014) was formally reported on December 25, 2013, with the manufacturer initiating the action on October 30, 2013. It is classified under Moderate severity (Class II), with a current status of Terminated. National Enzyme Co is listed as the recalling firm, operating out of Forsyth, MO. Federal records list the affected scope as 14519 bottles and 50000 bulk capsules.
The documented reason for this recall is: Firm is recalling dietary supplements containing a raw material which may contain >0.3 ppb chloramphenicol Distribution data in the federal record shows the product reached: 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, Nor…. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 6 from FDA Food — clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Food recalls over time
Where this recall sits in its category — 25,414 food recalls on record
Where this recall sits in the database
Of 100,165 recalls in the database, 23,668 are high severity, 72,097 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
14519 bottles and 50000 bulk capsules
Related Recalls
6
6 from same agency
Product description
Dietary Supplements packaged in the following configurations: (1) Houston Enzymes, No-Fenol, Multi-Enzyme Product for Digestion of Phenolic Foods and Fiber packaged in 90-capsule bottles (SKU 52437). Firm name on the label is Houston Nutraceuticals, Inc. (HNI), Siloam, AR; (2) 5327 Houston NO-FENOL blk 1v, Bulk Capsules (SKU 91456)
Reason for recall
Firm is recalling dietary supplements containing a raw material which may contain >0.3 ppb chloramphenicol
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-0745-2014 |
| Date reported | December 25, 2013 |
| Date initiated | October 30, 2013 |
| Recalling firm | National Enzyme Co |
| Firm location | Forsyth, MO |
| Affected scope | 14519 bottles and 50000 bulk capsules |
| 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… |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (F-0745-2014) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting — recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
Dietary Supplements packaged in the following configurations: (1) Houston Enzymes, No-Fenol, Multi-Enzyme Product for Digestion of Phenolic Foods and Fiber packaged in 90-capsule bottles (SKU 52437). Firm name on the label is Houston Nutraceuticals, Inc. (HNI), Siloam, AR; (2) 5327 Houston NO-FENOL blk 1v, Bulk Capsules (SKU 91456). Recalled by National Enzyme Co. Units affected: 14519 bottles and 50000 bulk capsules.
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-0745-2014.
Where was the recalled product distributed? ▼
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..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-0745-2014) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
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Data Sources
Source: FDA, CPSC, and NHTSA federal recall databases. This recall: FDA Food, reported December 25, 2013.
- Source: FDA — Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
- Source: CPSC — Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
- Source: NHTSA — National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)
Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of June 2026.