Severity
Moderate
FDA Food recall · Reported April 6, 2016
NatureMed Inc. dba Institute for Vibrant Living is recalling All Day Energy Greens powdered green drink due to some reported cases of gastrointestinal distress.
Naturmed Inc DBA Institute for Vibrant Living recalled All Day Energy Greens Fruity (ADEGF), Great Fruity Taste!, Net Wt 10.5 oz (299g), UPC Cod… - a moderate-severity action.
All Day Energy Greens Fruity (ADEGF), Great Fruity Taste!, Net Wt 10.5 oz (299g), UPC Cod… was recalled by Naturmed Inc DBA Institute for Vibrant Living in April 6, 2016. Reason: NatureMed Inc. dba Institute for Vibrant Living is recalling All Day Energy Greens powdered green drink due t…. Check the official notice for the remedy. Verify recall #F-1006-2016 with the FDA Food before acting.
The recall
Naturmed Inc DBA Institute for Vibrant Living issued this moderate-severity FDA Food recall-NatureMed Inc. dba Institute for Vibrant Living is recalling All Day Energy Greens powdered green drink due t….
Sourced from official FDA Food enforcement records. Verify recall #F-1006-2016 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Food action (record #F-1006-2016) was formally reported on April 6, 2016, with the manufacturer initiating the action on March 11, 2016. It is classified under Moderate severity (Class II), with a current status of Terminated. Naturmed Inc DBA Institute for Vibrant Living is listed as the recalling firm, operating out of Camp Verde, AZ. Federal records list the affected scope as 376,878 units, a scale large enough to require multi-state distribution tracking.
The documented reason for this recall is: NatureMed Inc. dba Institute for Vibrant Living is recalling All Day Energy Greens powdered green drink due to some reported cases of gastrointestinal distress. Distribution data in the federal record shows the product reached: US. 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.
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 moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Moderate
Affected scope
376,878 units
Related Recalls
6
6 from same agency
All Day Energy Greens Fruity (ADEGF), Great Fruity Taste!, Net Wt 10.5 oz (299g), UPC Code 893320002096 and 893320002423.
NatureMed Inc. dba Institute for Vibrant Living is recalling All Day Energy Greens powdered green drink due to some reported cases of gastrointestinal distress.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-1006-2016 |
| Date reported | April 6, 2016 |
| Date initiated | March 11, 2016 |
| Recalling firm | Naturmed Inc DBA Institute for Vibrant Living |
| Firm location | Camp Verde, AZ |
| Affected scope | 376,878 units |
| Distribution | US |
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.
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.
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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 April 6, 2016. 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.