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RECALL RECORD — CLASS IIRecall closedF-1006-2016/FDA enforcement
Naturmed INC Dba Institute for Vibrant Living·Food·Mar 11, 2016

All Day Energy Greens Fruity (Adegf), Great Fruity Taste!, NET WT 10.5 OZ (299g)

What you need to know

Class II

  • What happened

    NatureMed Inc. dba Institute for Vibrant Living is recalling All Day Energy Greens powdered green drink due to some reported cases of gastrointestinal distress.

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • Action required

    Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice.

Recall closed · classified by the FDADistribution not listedMore food

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Product identification

Source: FDA FOOD

Brand nameNaturmed INC Dba Institute for Vibrant Living
Recalling firmNaturmed INC Dba Institute for Vibrant LivingCamp Verde, AZ, United States
UPC / barcodes
8 93320 00209 68 93320 00242 3
Lot / date codes
  • 1405460 1405461 1405462 1405463 1405464 1405465 1405466 1405467 1407114 1407115 1407116 1407117 1407118 1407119 1412332 1412333 1412337 1412334 1412335 1412336 1412338 1412339 1412340 1412341 1412415 1412416 1412417 1412418 1412419 1412420 1412421 1505180 1505181 1505182 1505183
Distribution area

US

United States

Quantity affected376, 878 units
Recall initiationFDA report date: April 6, 2016
FDA recall numberF-1006-2016

Beyond the headline

The recall, in context

Naturmed INC Dba Institute for Vibrant Living initiated this food recall on March 11, 2016. The FDA enforcement report states: NatureMed Inc. dba Institute for Vibrant Living is recalling All Day Energy Greens powdered green drink due to some reported cases of gastrointestinal distress. The FDA report lists distribution as: US.

The FDA enforcement report describes the reason as: NatureMed Inc. dba Institute for Vibrant Living is recalling All Day Energy Greens powdered green drink due to some reported cases of gastrointestinal distress.

All Day Energy Greens Fruity (Adegf), Great Fruity Taste!, NET WT 10.5 OZ (299g) was made or distributed by Naturmed INC Dba Institute for Vibrant Living in Camp Verde, AZ, United States. This page reflects FDA report F-1006-2016, dated April 6, 2016.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the UPC and lot code against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Product safety recall

Symptoms to watch for

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Higher-risk groups

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What to do now

  1. 1Stop using or eating the product and keep it away from children and pets.
  2. 2Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return.
  3. 3Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Read the official source record for the specific hazard and instructions.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the All Day Energy Greens Fruity (Adegf), Great Fruity Taste!, NET WT 10.5 OZ (299g) recall?

Naturmed INC Dba Institute for Vibrant Living recalled All Day Energy Greens Fruity (Adegf), Great Fruity Taste!, NET WT 10.5 OZ (299g) in an FDA Class II enforcement action reported as F-1006-2016. NatureMed Inc. dba Institute for Vibrant Living is recalling All Day Energy Greens powdered green drink due to some reported cases of gastrointestinal distress.

What should I do if I bought this product?

Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice. Stop using or eating the product and keep it away from children and pets. Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return. Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Is the Naturmed INC Dba Institute for Vibrant Living recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-1006-2016. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

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Naturmed INC Dba Institute for Vibrant Living

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NatureMed Inc. dba Institute for Vibrant Living is recalling All Day Energy Greens powdered green drink due to some reported cases of gastrointestinal distress.

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.