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
Class I - DangerousWhat Should You Do?
- Check if you have this product: Lot Numbers: A. 1401084 B. 1401083, 1401092, 1401094 C. 1401081, 1401082, 1401085, 1401086, 1401087, 1401088,1401089 D. 1401079, 1401080, 1401081
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Vibrant Health
- Reason for Recall:
- A raw material used in the manufacture of the dietary supplements was found to contain Salmonella bacteria.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full 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
Product Codes/Lot Numbers:
Lot Numbers: A. 1401084 B. 1401083, 1401092, 1401094 C. 1401081, 1401082, 1401085, 1401086, 1401087, 1401088,1401089 D. 1401079, 1401080, 1401081
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: F-2434-2014
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