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
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
- Brand
- Energique Mineral
- 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 2024 | Recall initiated by company | |
| 2 Jul 2024 | Classified by FDA | +60 days |
| 10 Jul 2024 | Published 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
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| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS II | BioActive Nutritional Minaplex, Botanical Herbal Supplement recalledBioActive Nutritional | Grato Holdings | Mold | Nationwide |
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|---|---|---|---|---|---|
| Food | CLASS II | BioActive Nutritional Minaplex, Botanical Herbal Supplement recalledBioActive Nutritional | Grato Holdings | Mold | Nationwide |
| Drug | CLASS III | V-force Homeopathic recalled by Grato Holdings | Grato Holdings | Packaging Defects | FL |
| Drug | CLASS II | Earache Drops recalled by Grato HoldingsWalgreens Earache Drops | Grato Holdings | Sterility | Nationwide |
| Drug | CLASS II | Homeopathic EarAche Ear Drops recalled by Grato Holdings | Grato Holdings | Sterility | Nationwide |
| Drug | CLASS II | Homeopathic EarAche Drops recalled by Grato HoldingsEar Care Earache Drops | Grato Holdings | Sterility | Nationwide |
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