Green Vibrance- A Comprehensive Restorative Advanced Daily Superfood (Dietary Supplement) packaged as follows: A. 15-day, 181.5g, 6.4 oz. powder- Product Code GV15; B. 30-day, 363g, 12.8 oz. powder; Product Code GV 30; C.60-day, 726g, 25.61 oz. family size powder, -Product Code GV60; D. Bulk Supply Kilo Canister, 1 kg (35.27 oz.) powder,-Product Code GVKG
Recalled by Vibrant Health on Jul 25, 2014
Reason for Recall
A raw material used in the manufacture of the dietary supplements was found to contain Salmonella bacteria.
Product Description
Green Vibrance- A Comprehensive Restorative Advanced Daily Superfood (Dietary Supplement) packaged as follows: A. 15-day, 181.5g, 6.4 oz. powder- Product Code GV15; B. 30-day, 363g, 12.8 oz. powder; Product Code GV 30; C.60-day, 726g, 25.61 oz. family size powder, -Product Code GV60; D. Bulk Supply Kilo Canister, 1 kg (35.27 oz.) powder,-Product Code GVKG
Distribution
Nationwide OUS: UK, Iceland, South Africa
What Should You Do?
- 1.Check your kitchen for this product immediately.
- 2.Do not consume the recalled product.
- 3.Return the product to where you bought it for a full refund, or throw it away.
- 4.If you have experienced any health issues, contact your healthcare provider.
Browse Related Recalls
Terms Explained
- Salmonella — learn what this means in food safety
- Class I Recall — learn what this means in food safety
- FDA Food Recall — learn what this means in food safety
The this entity record above pulls directly from the FDA openFDA enforcement-report API. What follows is the per-entity context — how this entity sits in the broader U.S. FDA food, drug, and device recalls distribution and which underlying factors drive the headline numbers.
Every number on this page links back to the FDA openFDA enforcement-report API; the methodology page describes the inputs, refresh cadence, and known limitations of the underlying data product.
Practical use of this page is in combination with the comparison and ranking pages elsewhere on the site, which surface the same data for this entity’s peers within U.S. consumer-product recalls. A single-entity reading without peer context can be misleading when an entity is an outlier on one axis but typical on another.
Source: FDA Recalls, Market Withdrawals and Safety Alerts, 2026.