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Food recall · FDA · Published April 16, 2018

Grato Holdings, Inc. recalls Energique, Herbal Supplement, Octocom,; Dist. by Energique, Inc. Woodbine, IA 51579

Grato Holdings recalls Energique herbal supplements due to unapproved drug claims. Products marketed as dietary supplements with disease-related health claims are illegal under FDA regulations.

🇺🇸 FDA recall #F-1401-2018FoodGrato Holdings ›
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Contact the company & request your remedy

Recalling firmGrato Holdings, Inc.201 Apple Blvd, N/A · Woodbine, IA 51579-1503
No email on file for this recall — reach the company by phone or its official page instead.No email on file — write to the address above instead.
✎ GovInfoNow plain-language explainer

What happened, in plain English

Grato Holdings is recalling several Energique herbal supplements because they are marketed as dietary supplements but contain unapproved drug claims. This means the products could be illegal under FDA regulations and pose health risks if used without proper medical supervision. Read more at govinfonow.com/recall/19209-grato-holdings-energique-herbal-supplement-recall-unapproved-drug-claims.

Source Summary by GovInfoNow · govinfonow.com/recall/19209-grato-holdings-energique-herbal-supplement-recall-unapproved-drug-claims · Updated October 7, 2026 · FDA enforcement record: FDA #F-1401-2018

Cite this page

“Grato Holdings Energique Herbal Supplement Recall: Unapproved Drug Claims.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19209-grato-holdings-energique-herbal-supplement-recall-unapproved-drug-claims. Based on FDA recall #F-1401-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1401-2018%22&limit=1).

Why it’s dangerous

These supplements are marketed as dietary supplements but contain claims about treating diseases or using drug-like methods. The FDA considers such claims as unapproved drug activities, which can be risky if the product is used without medical guidance.

Who’s affected

People who purchased Energique herbal supplements from the listed product codes. Those with health conditions or using supplements for disease treatment are at higher risk.

How to tell if you have this one

Check product labels for the codes J20597, J20840, J21846, J21849, J21850, J23464, J23465, J23466, or J23467. Products distributed by Energique, Inc. in Woodbine, IA are affected.

  • Brand
    Grato Holdings
  • Category
    Food
FDA recall event · 4 products

All 4 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
    Shipped to customers nationwide and Canada.
Recall numberProduct, codes & lotsQuantity
F-1400-2018Peaceful Mountain -Stomach Rescue - Dietary supplement - Elemental silver (45 ppm) 2.7 mg; Dist. by Peaceful Mountain, Inc. Woodbine, IA 51579; G9525, G9706, G9980, G10419, G1064132,213 4 oz packages
F-1401-2018Energique, Herbal Supplement, Octocom,; Dist. by Energique, Inc. Woodbine, IA 51579; J20597, J20840, J21846, J21849, J21850, J23464, J23465, J23466, J23467845 1-oz bottles, 59 1-oz bottles
F-1402-2018Peaceful Mountain, Nasal Rescue, Dietary Supplement, Natural Sinus Support, Dist. by Peaceful Mountain, Inc. Woodbine, IA 51579; G9558, G9716, G10110, G1047127,860 1.5 oz bottles
F-1403-2018Energique, Dietary Supplement, Enervimin CNCR Focus, Dist. by Energique Inc.. Woodbine, IA 51579; 50070340, 55837004767 120-tablet bottles
Based on the official FDA remedy

What to do — step by step

  1. Check Product Labels

    Look for the specific product codes listed in the recall notice to identify affected items.

✎ GovInfoNow

Questions people ask

Are these products safe to use?

The recall states these products are unapproved drugs based on disease claims, so they may pose health risks. Consult a healthcare provider before use.

How can I tell if I have an affected product?

Check the product label for the codes J20597, J20840, J21846, J21849, J21850, J23464, J23465, J23466, or J23467.

What should I do if I have an affected product?

The recall does not specify a remedy, so contact the manufacturer or healthcare provider for guidance.

Take action

Contact Grato Holdings

We’ve drafted a message you can send Grato Holdings to request your refund or repair — edit it as you like.

Subject: Recall F-1401-2018 — Grato Holdings Grato Holdings

Hello,

I own a Grato Holdings that is covered by recall F-1401-2018 from Grato Holdings.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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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-1401-2018 (April 16, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1401-2018 to see it in context.
  • Plain-language summary written by qwen3:4b on October 7, 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