Food recall: Green Vibrance- A Comprehensive Restorative Advanced Daily Superfood (Dietary Supplement) packaged as follows: A. 15-day
FDA enforcement event 68949 is a food recall by Vibrant Health of Canaan, CT, initiated 25 Jul 2014 and classified Class I, with 4 product records.
FDA defines Class I as a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death. 50% of the 573 food enforcement events initiated in 2014 carry the same class.
Status: Terminated, terminated 21 Apr 2015. Initiation: voluntary: firm initiated. This is the only enforcement event on this register for Vibrant Health.
Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.
Recalling firm
Vibrant Health, Canaan, CT.
Reason for recall
"A raw material used in the manufacture of the dietary supplements was found to contain Salmonella bacteria."
Distribution
"Nationwide OUS: UK, Iceland, South Africa"
Product records
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| F-2434-2014 | 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… | 44,257 units | Class I | Terminated | 24 Sep 2014 |
| F-2435-2014 | Green Vibrance 15 single serve pkts, 181.5g, 6.4oz. Product Code: GVSD | 8,726 | Class I | Terminated | 24 Sep 2014 |
| F-2436-2014 | Green Vibrance, 240 Vegicaps/bottle Product Code: GVC | 5,355 | Class I | Terminated | 24 Sep 2014 |
| F-2437-2014 | Rainbow Vibrance Hi ORAC Superfood, 177g, 6.24 oz. Product Code: RV | 5,164 | Class I | Terminated | 24 Sep 2014 |
Context
Questions and answers
Why was this food recalled?
FDA's record gives the reason for recall as: "A raw material used in the manufacture of the dietary supplements was found to contain Salmonella bacteria."
What does Class I mean?
FDA classifies recalls by relative degree of health hazard. Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.
Where was the product distributed?
FDA's distribution pattern field reads: "Nationwide OUS: UK, Iceland, South Africa"
Is the recall still ongoing?
FDA lists the status as Terminated; the termination date is 21 Apr 2015. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.
Where does this data come from?
openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.
Provenance
Source: openFDA food enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.