Colon Rebuild I (90 capsules), 2boxes x 240 bottles, 1box x 200 bottles.
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1635-2014.
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.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1635-2014.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Global Vitality, Inc. Dba Enzyme Process International or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- If you've been hurt by this product, report the incident to FDA.
Consumer Contact (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1635-2014.
Global Vitality, Inc. dba Enzyme Process International
About the U.S. Food and Drug Administration
The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
Visit FDA.gov →📣 Report a food, supplement, or cosmetic problem to the FDA
If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.
Global Vitality, Inc. Dba Enzyme Process International Recall FAQ
Global Vitality, Inc. Dba Enzyme Process International is the subject of a food safety report: Colon Rebuild I (90 capsules), 2boxes x 240 bottles, 1box x 200 bottles.. The notice was published on October 22, 2013 by the U.S. Food and Drug Administration (FDA). Approximately 63,180 units are potentially affected.