PlainRecalls
ModerateClass IITerminated

FDA Food recall · Reported February 5, 2014

Enzyme Formula, dietary supplement, 100 capsules or 250 capsules per bottles, sold unlabeled to Rich Distributing.

Dietary supplement products are recalled because they were made from ingredient that was contaminated with Chloramphenicol.

Recall #
F-1459-2014
Affected scope
200 bottles (100 ct); 367 bottles (250 ct)
Initiated
October 25, 2013
Verify with FDA Food →
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Health Wright Products Inc recalled Enzyme Formula, dietary supplement, 100 capsules or 250 capsules per bottles, sold unlabe… — a moderate-severity action.

Enzyme Formula, dietary supplement, 100 capsules or 250 capsules per bottles, sold unlabe… was recalled by Health Wright Products Inc in February 5, 2014. Reason: Dietary supplement products are recalled because they were made from ingredient that was contaminated with Ch…. Check the official notice for the remedy. Verify recall #F-1459-2014 with the FDA Food before acting.

The recall

Health Wright Products Inc issued this moderate-severity FDA Food recall — Dietary supplement products are recalled because they were made from ingredient that was contaminated with Ch….

Moderate
severity level
Class II
classification
February 5, 2014
reported

Sourced from official FDA Food enforcement records. Verify recall #F-1459-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This FDA Food action (record #F-1459-2014) was formally reported on February 5, 2014, with the manufacturer initiating the action on October 25, 2013. It is classified under Moderate severity (Class II), with a current status of Terminated. Health Wright Products Inc is listed as the recalling firm, operating out of Clackamas, OR. Federal records list the affected scope as 200 bottles (100 ct); 367 bottles (250 ct).

The documented reason for this recall is: Dietary supplement products are recalled because they were made from ingredient that was contaminated with Chloramphenicol. Distribution data in the federal record shows the product reached: Distributed to California, Florida, Oregon, Utah, and Mexico. 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, 1 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.

Drugs & Medications recalls over time

Where this recall sits in its category — 14,048 drugs & medications recalls on record

-50005001,0001,5002,000 20052009201220152018202120242026 216

Where this recall sits in the database

Severity2366872097High severity (most serious)Moderate severityLow severity
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.

Severity

Moderate

Affected scope

200 bottles (100 ct); 367 bottles (250 ct)

Related Recalls

6

1 from same agency

Product description

Enzyme Formula, dietary supplement, 100 capsules or 250 capsules per bottles, sold unlabeled to Rich Distributing.

Reason for recall

Dietary supplement products are recalled because they were made from ingredient that was contaminated with Chloramphenicol.

Recall Profile

Structured summary of the FDA Food recall record
Attribute Value
Agency U.S. Food and Drug Administration
Severity class Moderate (Class II)
Status Terminated
Recall number F-1459-2014
Date reported February 5, 2014
Date initiated October 25, 2013
Recalling firm Health Wright Products Inc
Firm location Clackamas, OR
Affected scope 200 bottles (100 ct); 367 bottles (250 ct)
Distribution Distributed to California, Florida, Oregon, Utah, and Mexico

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-1459-2014) 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?
Enzyme Formula, dietary supplement, 100 capsules or 250 capsules per bottles, sold unlabeled to Rich Distributing.. Recalled by Health Wright Products Inc. Units affected: 200 bottles (100 ct); 367 bottles (250 ct).
Why was this product recalled?
Dietary supplement products are recalled because they were made from ingredient that was contaminated with Chloramphenicol.
Which agency issued this recall?
This recall was issued by the FDA Food on February 5, 2014. Severity: Moderate. Recall number: F-1459-2014.
Where was the recalled product distributed?
Distribution: Distributed to California, Florida, Oregon, Utah, and Mexico.
How do I check if my product is affected by a recall?
Check the product description and recall number (F-1459-2014) 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.

Nearby Recalls in This Category

Other recalls in the same product category — useful for spotting patterns across the same defect class or manufacturer.

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Data Sources

Source: FDA, CPSC, and NHTSA federal recall databases. This recall: FDA Food, reported February 5, 2014.

  • 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.