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Global Vitality, Inc. dba Enzyme Process International

Complete recall history across all FDA and CPSC categories — 9 total recalls

Global Vitality, Inc. dba Enzyme Process International appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Food Recalls (9)

FDA food safety enforcement actions by Global Vitality, Inc. dba Enzyme Process International

Date Product Reason Class
Oct 22, 2013 Energy Clarity (bulk), 6 boxes x 15 kg, 1 box x 10.55 kg. Global Vitality is recalling dietary supplements because they may be contamin... Class II
Oct 22, 2013 Adrenal Support (bulk), 4 boxes x 12 kg, 1 box x 11.48 kg. Global Vitality is recalling dietary supplements because they may be contamin... Class II
Oct 22, 2013 Total Digestion, Lot 1635, 4 boxes x 9.92 kg. Lot 1841, 4 boxes x 12 kg, 1... Global Vitality is recalling dietary supplements because they may be contamin... Class II
Oct 22, 2013 Fat Sugar (bulk), 3 boxes x 12 kg, 1 box x 8.76 kg. Global Vitality is recalling dietary supplements because they may be contamin... Class II
Oct 22, 2013 Multi Vitamin (bulk), 6 boxes x 12 kg, 1 box x 5.5kg. Global Vitality is recalling dietary supplements because they may be contamin... Class II
Oct 22, 2013 Super Digestayme, 200 count, 2 boxes x 72 bottles, 1 box x 55 bottles. 300 co... Global Vitality is recalling dietary supplements because they may be contamin... Class II
Oct 22, 2013 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 contamin... Class II
Oct 22, 2013 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 contamin... Class II
Oct 22, 2013 Colon Rebuild I (90 capsules), 2boxes x 240 bottles, 1box x 200 bottles. Global Vitality is recalling dietary supplements because they may be contamin... Class II

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

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