Severity
Moderate
ModerateClass IITerminated
FDA Food recall · Reported March 19, 2014
Colon Rebuild I (90 capsules), 2boxes x 240 bottles, 1box x 200 bottles.
Global Vitality is recalling dietary supplements because they may be contaminated with chloramphenicol. The dietary supplements were made with a raw ingredient that was on recall…
The recall
Global Vitality, Inc. dba Enzyme Process International issued this moderate-severity FDA Food recall — Global Vitality is recalling dietary supplements because they may be contaminated with chloramphenicol. The ….
- Moderate
- severity level
- 63K units
- affected scope
- Class II
- classification
- March 19, 2014
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-1635-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-1635-2014) was formally reported on March 19, 2014, with the manufacturer initiating the action on October 22, 2013. It is classified under Moderate severity (Class II), with a current status of Terminated. Global Vitality, Inc. dba Enzyme Process International is listed as the recalling firm, operating out of Chandler, AZ. Federal records list the affected scope as 63,180 units.
The documented reason for this recall is: Global Vitality is recalling dietary supplements because they may be contaminated with chloramphenicol. The dietary supplements were made with a raw ingredient that was on recalled by Specialty Enzymes & Biotechnologie… Distribution data in the federal record shows the product reached: PA, AZ, HI,. 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
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.
Affected scope
63,180 units
Related Recalls
6
1 from same agency
Product description
Colon Rebuild I (90 capsules), 2boxes x 240 bottles, 1box x 200 bottles.
Reason for recall
Global Vitality is recalling dietary supplements because they may be contaminated with chloramphenicol. The dietary supplements were made with a raw ingredient that was on recalled by Specialty Enzymes & Biotechnologies due to chloramphenicol.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-1635-2014 |
| Date reported | March 19, 2014 |
| Date initiated | October 22, 2013 |
| Recalling firm | Global Vitality, Inc. dba Enzyme Process International |
| Firm location | Chandler, AZ |
| Affected scope | 63,180 units |
| Distribution | PA, AZ, HI, |
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-1635-2014) 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? ▼
Colon Rebuild I (90 capsules), 2boxes x 240 bottles, 1box x 200 bottles.. Recalled by Global Vitality, Inc. dba Enzyme Process International. Units affected: 63,180 units.
Why was this product recalled? ▼
Global Vitality is recalling dietary supplements because they may be contaminated with chloramphenicol. The dietary supplements were made with a raw ingredient that was on recalled by Specialty Enzymes & Biotechnologies due to chloramphenicol.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on March 19, 2014. Severity: Moderate. Recall number: F-1635-2014.
Where was the recalled product distributed? ▼
Distribution: PA, AZ, HI,.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-1635-2014) 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 March 19, 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.