CLASS II Food recall · Reported 10 Jul 2024 · FDA Enforcement Report

Energique Mineral Magic Dietary Supplement recalled by Grato Holdings

Grato Holdings is recalling Energique Mineral Magic Dietary Supplement, distributed nationwide in the US. The recall was initiated on 3 May 2024 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot: G11602 MFD: 06/21; Lot G11747 MFD: 07/22; Lot: G11723 MFD 08/22
Quantity recalled1912 bottles

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-1458-2024
FDA event ID
94577
Recalling firm
Grato Holdings, Woodbine, IA
Classification
Class II
Status
Terminated
Recall initiated
3 May 2024
FDA classified
2 Jul 2024
Reported
10 Jul 2024
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Mold
Product category
Dietary Supplements

Timeline

3 May 2024Recall initiated by company
2 Jul 2024Classified by FDA+60 days
10 Jul 2024Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Potential microbial contamination (yeast and/or mold).

Product as listed by the FDA

Energique Mineral Magic Dietary Supplement, 2 fl. oz (59 ml) bottle.

Where it was distributed

Nationwide US and Canada

Nationwide

Questions about this recall

Why was it recalled?

Potential microbial contamination (yeast and/or mold).

Which lots are affected?

Lot: G11602 MFD: 06/21; Lot G11747 MFD: 07/22; Lot: G11723 MFD 08/22

Where was it sold?

Nationwide US and Canada

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

1 other product · FDA event 94577
ReportedClassRecallCompanyReasonWhere
CLASS IIBioActive Nutritional Minaplex, Botanical Herbal Supplement recalledBioActive NutritionalGrato HoldingsMoldNationwide

More recalls from Grato Holdings

All 18
ReportedClassRecallCompanyReasonWhere
FoodCLASS IIBioActive Nutritional Minaplex, Botanical Herbal Supplement recalledBioActive NutritionalGrato HoldingsMoldNationwide
DrugCLASS IIIV-force Homeopathic recalled by Grato HoldingsGrato HoldingsPackaging DefectsFL
DrugCLASS IIEarache Drops recalled by Grato HoldingsWalgreens Earache DropsGrato HoldingsSterilityNationwide
DrugCLASS IIHomeopathic EarAche Ear Drops recalled by Grato HoldingsGrato HoldingsSterilityNationwide
DrugCLASS IIHomeopathic EarAche Drops recalled by Grato HoldingsEar Care Earache DropsGrato HoldingsSterilityNationwide

Other Dietary Supplements recalls

All 733