Severity
Critical
CriticalClass ITerminated
FDA Food recall · Reported September 24, 2014
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
A raw material used in the manufacture of the dietary supplements was found to contain Salmonella bacteria.
Vibrant Health recalled Green Vibrance- A Comprehensive Restorative Advanced Daily Superfood (Dietary Supplement)… - a critical-severity action.
Green Vibrance- A Comprehensive Restorative Advanced Daily Superfood (Dietary Supplement)… was recalled by Vibrant Health in September 24, 2014. Reason: A raw material used in the manufacture of the dietary supplements was found to contain Salmonella bacteria.. Check the official notice for the remedy. Verify recall #F-2434-2014 with the FDA Food before acting.
The recall
Vibrant Health issued this critical-severity FDA Food recall-A raw material used in the manufacture of the dietary supplements was found to contain Salmonella bacteria..
- Critical
- severity level
- 44K units
- affected scope
- Class I
- classification
- September 24, 2014
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-2434-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-2434-2014) was formally reported on September 24, 2014, with the manufacturer initiating the action on July 25, 2014. It is classified under Critical severity (Class I), with a current status of Terminated. Vibrant Health is listed as the recalling firm, operating out of Canaan, CT. Federal records list the affected scope as 44,257 units.
The documented reason for this recall is: A raw material used in the manufacture of the dietary supplements was found to contain Salmonella bacteria. Distribution data in the federal record shows the product reached: Nationwide OUS: UK, Iceland, South Africa. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 6 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Dietary Supplements recalls over time
Where this recall sits in its category - 2,002 dietary supplements recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified high severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
44,257 units
Related Recalls
6
6 from same agency
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
Reason for recall
A raw material used in the manufacture of the dietary supplements was found to contain Salmonella bacteria.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Terminated |
| Recall number | F-2434-2014 |
| Date reported | September 24, 2014 |
| Date initiated | July 25, 2014 |
| Recalling firm | Vibrant Health |
| Firm location | Canaan, CT |
| Affected scope | 44,257 units |
| Distribution | Nationwide OUS: UK, Iceland, South Africa |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (F-2434-2014) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- This is a Class I (high-risk) recall, stop using the product immediately and follow the disposal or return instructions. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
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. Units affected: 44,257 units.
Why was this product recalled? ▼
A raw material used in the manufacture of the dietary supplements was found to contain Salmonella bacteria.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on September 24, 2014. Severity: Critical. Recall number: F-2434-2014.
Where was the recalled product distributed? ▼
Distribution: Nationwide OUS: UK, Iceland, South Africa.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-2434-2014) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Compare this recall with Blue Bull Extreme Male Enhancement Supplement, total of 15 … →
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported September 24, 2014. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.