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Use caution Food recall · FDA · Published March 11, 2016

Naturmed All Day Energy Greens Recall: GI Distress Risk

Naturmed recalls All Day Energy Greens Fruity powdered drink due to reported gastrointestinal distress. Check UPCs and lot codes for details.

🇺🇸 FDA recall #F-1006-2016FoodNaturmed ›
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Recalling firmNaturmed Inc DBA Institute for Vibrant Living661 E Howards Rd Ste C · Camp Verde, AZ 86322-6521
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What happened, in plain English

Naturmed Inc., doing business as Institute for Vibrant Living, is recalling All Day Energy Greens Fruity powdered green drink because some consumers have reported gastrointestinal distress. The recall covers approximately 376,878 units distributed across the United States. No specific remedy or return instructions are currently provided in the record. Read more at govinfonow.com/recall/25057-naturmed-all-day-energy-greens-recall-gi-distress-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/25057-naturmed-all-day-energy-greens-recall-gi-distress-risk · Updated October 11, 2026 · FDA enforcement record: FDA #F-1006-2016

Cite this page

“Naturmed All Day Energy Greens Recall: GI Distress Risk.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/25057-naturmed-all-day-energy-greens-recall-gi-distress-risk. Based on FDA recall #F-1006-2016 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1006-2016%22&limit=1).

Why it’s dangerous

The product is being recalled due to reported cases of gastrointestinal distress among consumers who drank it. The specific cause of the distress is not detailed in the record, but the symptom indicates a potential health issue associated with the product.

Who’s affected

Consumers who purchased All Day Energy Greens Fruity powdered green drink with a net weight of 10.5 oz (299g) and sold in the United States are affected. Individuals experiencing gastrointestinal distress after consumption may be at risk.

How to tell if you have this one

Check your container for the brand name 'All Day Energy Greens Fruity' and the description 'Great Fruity Taste!'. Verify the net weight is 10.5 oz (299g). Look for UPC codes 893320002096 or 893320002423, and lot codes including 1405460 through 1405467, 1407114 through 1407119, 1412332 through 1412341, 1412415 through 1412421, and 1505180 through 1505183.

  • Brand
    Naturmed
  • Product
    All Day Energy Greens Fruity (ADEGF), Great Fruity Taste!, Net Wt 10.5 oz (299g), UPC Code 893320002096 and
  • Category
    Food
FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Terminated
  • Distribution
    US
Recall numberProduct, codes & lotsQuantity
F-1005-2016All Day Energy Greens (ADEG), Original Flavor, Net Wt 11.36 oz (322g), UPC Code 893320002096; 1406027 1406028 1406029 1406030 1406326 1406327 1406328 1406329 1406330 1406331 1406332 1406333 1406334 1406335 1406338 1406339 1406340 1406341 1406398 1406399 1406400 1406401 1406402 1406403 1412322 1412323 1412324 1412325 1412326 1412327 1412328 1412329 1412330 1412331 1412406 1412407 1412408 1412409 1412410 1412411 1412412 1412413 1501255 1501256 1501257 1501258 1505189 1505190 1505191563,499 units
F-1006-2016All Day Energy Greens Fruity (ADEGF), Great Fruity Taste!, Net Wt 10.5 oz (299g), UPC Code 893320002096 and 893320002423.; 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 1505183376,878 units
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Verify if your product matches the UPC codes 893320002096 or 893320002423 and one of the listed lot codes.

  2. Monitor Health Symptoms

    Be aware of any gastrointestinal distress after consuming the product, as this is the reported hazard.

How this recall unfolded

Recall timeline

FDA terminated this recall 7 months after the firm started it.

1. Firm started the recall: Mar 11, 201612. FDA classified it Class II: Mar 30, 201623. Published in FDA’s Enforcement Report: Apr 6, 201634. FDA terminated the recall: Oct 4, 201642016
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Questions people ask

Which lot codes are included in the recall?

Affected lot codes include 1405460-1405467, 1407114-1407119, 1412332-1412341, 1412415-1412421, and 1505180-1505183.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #F-1006-2016 (March 11, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1006-2016 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 11, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA