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Stop using now Food recall · FDA · Published May 3, 2024

Energique Mineral Magic Recall: Microbial Contamination Risk

Grato Holdings recalls Energique Mineral Magic dietary supplement due to potential yeast and mold contamination. Check your lot numbers immediately.

🇺🇸 FDA recall #F-1458-2024FoodEnergique ›
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Recalling firmGrato Holdings, Inc.201 Apple Blvd · Woodbine, IA 51579-1503
✎ GovInfoNow plain-language explainer

Grato Holdings, Inc. is recalling Energique Mineral Magic Dietary Supplement in 2 fl. oz bottles because of potential microbial contamination by yeast and/or mold. The recall covers specific lots manufactured between June and August 2021. Consumers should check their product labels to see if they are affected. Read more at govinfonow.com/recall/9322-energique-mineral-magic-recall-microbial-contamination-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/9322-energique-mineral-magic-recall-microbial-contamination-risk · Updated October 9, 2026 · FDA enforcement record: FDA #F-1458-2024

Cite this page

“Energique Mineral Magic Recall: Microbial Contamination Risk.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/9322-energique-mineral-magic-recall-microbial-contamination-risk. Based on FDA recall #F-1458-2024 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1458-2024%22&limit=1).

Grato Holdings, Inc. voluntarily recalled Energique Mineral Magic Dietary Supplement due to potential microbial contamination of yeast and/or mold, the FDA announced on May 3, 2024. The Food and Drug Administration issued recall number F-1458-2024 for the product.

How to tell if you have it

  • Brand: Energique
  • Product: Mineral Magic Dietary Supplement
  • Size: 2 fl. oz (59 ml) bottle
  • Lot G11602 MFD: 06/21
  • Lot G11747 MFD: 07/22
  • Lot G11723 MFD 08/22

The hazard

The product poses a risk of potential microbial contamination involving yeast and/or mold. The FDA classified this as a Class II recall.

Context

GovInfoNow's records show Grato Holdings, Inc. has had 8 other recalls on record since December 22, 2015. Other recent recalls of similar products include Wellnov Joint Nourish Liquid Recall (April 23, 2026), Wellnov Liposomal D3+B12 Spray Recall (April 23, 2026) and Wellnov Liposomal Mens 50+ Liquid Multivitamin Drops Recall (April 23, 2026).

How to tell if you have this one

Look for Energique Mineral Magic Dietary Supplement in 2 fl. oz (59 ml) bottles. Check the label for Lot numbers G11602 (MFD: 06/21), G11747 (MFD: 07/22), or G11723 (MFD: 08/22).

  • Brand
    Energique
  • 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
    Nationwide US and Canada
Recall numberProduct, codes & lotsQuantity
F-1458-2024Energique Mineral Magic Dietary Supplement, 2 fl. oz (59 ml) bottle.; Lot: G11602 MFD: 06/21; Lot G11747 MFD: 07/22; Lot: G11723 MFD 08/221912 bottles
F-1459-2024BioActive Nutritional MINAPLEX, Botanical Herbal Supplement; 1 Fl. oz. (30 ml) bottle.; Lot J28761261 bottles
Based on the official FDA remedy

What to do — step by step

  1. Check Your Product Label

    Verify if your bottle matches the recalled lot numbers and manufacture dates.

  2. Stop Consumption Immediately

    Do not consume the product if it is part of the recalled lots due to contamination risk.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Nationwide US and Canada” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA terminated this recall 2 months after the firm started it.

1. Firm started the recall: May 3, 202412. FDA classified it Class II: Jul 2, 202423. FDA terminated the recall: Jul 5, 202434. Published in FDA’s Enforcement Report: Jul 10, 202442024
  1. Firm started the recall
  2. FDA classified it Class II
  3. FDA terminated the recall
  4. Published in FDA’s Enforcement Report

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

✎ GovInfoNow

Questions people ask

Where was this product sold?

The product was distributed nationwide in the US and Canada.

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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-1458-2024 (May 3, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1458-2024 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 9, 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