Enzyme Process International — FDA Recall History & Enforcement Records
Data Notice: Recall frequency varies by category and firm size; data is comparative and may not indicate actual brand safety or quality. See Methodology.
As of July 16, 2026, Enzyme Process International has 9 recorded FDA food enforcement actions in the openFDA database. Their most recent recall was on 22 Oct 2013. Enzyme Process International is categorized under Supplements & Specialty based on their predominant recall history.
Recall activity over time for Enzyme Process International
How serious are Enzyme Process International recalls?
FDA recall classifications by severity
Full FDA recall history for Enzyme Process International
All 9 FDA enforcement actions sourced from openFDA · Sorted by date, most recent first
| Date | Product | Reason | Class & Status |
|---|---|---|---|
| 22 Oct 2013Official FDA Notice | 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 | Class IITerminated |
| 22 Oct 2013Official FDA Notice | Pain Power, 100 vegetarian capsules, 55 boxes x 72 bottles, 1 box x 7 bottles. | Global Vitality is recalling dietary supplements because they may be contaminated with chloramphenicol. The dietary supplements were made with a raw | Class IITerminated |
| 22 Oct 2013Official FDA Notice | Colon Rebuild II, 210 capsules, 6 boxes x 72 bottles, 1 box x 70 bottles. | Global Vitality is recalling dietary supplements because they may be contaminated with chloramphenicol. The dietary supplements were made with a raw | Class IITerminated |
| 22 Oct 2013Official FDA Notice | Super Digestayme, 200 count, 2 boxes x 72 bottles, 1 box x 55 bottles. 300 count, 4 boxes x 72 bottles, 1 box x 12 bottl | Global Vitality is recalling dietary supplements because they may be contaminated with chloramphenicol. The dietary supplements were made with a raw | Class IITerminated |
| 22 Oct 2013Official FDA Notice | Multi Vitamin (bulk), 6 boxes x 12 kg, 1 box x 5.5kg. | Global Vitality is recalling dietary supplements because they may be contaminated with chloramphenicol. The dietary supplements were made with a raw | Class IITerminated |
| 22 Oct 2013Official FDA Notice | Fat Sugar (bulk), 3 boxes x 12 kg, 1 box x 8.76 kg. | Global Vitality is recalling dietary supplements because they may be contaminated with chloramphenicol. The dietary supplements were made with a raw | Class IITerminated |
| 22 Oct 2013Official FDA Notice | Total Digestion, Lot 1635, 4 boxes x 9.92 kg. Lot 1841, 4 boxes x 12 kg, 1 box x 11.24 kg. Lot 2017, 3 boxes x 10 kg | Global Vitality is recalling dietary supplements because they may be contaminated with chloramphenicol. The dietary supplements were made with a raw | Class IITerminated |
| 22 Oct 2013Official FDA Notice | Adrenal Support (bulk), 4 boxes x 12 kg, 1 box x 11.48 kg. | Global Vitality is recalling dietary supplements because they may be contaminated with chloramphenicol. The dietary supplements were made with a raw | Class IITerminated |
| 22 Oct 2013Official FDA Notice | Energy Clarity (bulk), 6 boxes x 15 kg, 1 box x 10.55 kg. | Global Vitality is recalling dietary supplements because they may be contaminated with chloramphenicol. The dietary supplements were made with a raw | Class IITerminated |
Where have Enzyme Process International recalls occurred?
States affected across all recorded FDA enforcement actions
Where does this recall data come from?
Verification required: FoodRecallFinder.com cannot verify the safety of individual food products in your possession. Always verify the current recall status at FDA.gov before disposing of or consuming a product.
Data sourced from the FDA Recall Enterprise System via openFDA API. This information is for educational purposes only and does not constitute health or legal advice. FoodRecallFinder.com is not affiliated with or endorsed by the U.S. Food and Drug Administration.
To determine if your specific product is affected, verify that the brand name, product description, lot number, UPC code, and date range all match the recall details exactly. When in doubt contact the recalling firm or visit FDA.gov.
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