Energique Mineral Magic Dietary Supplement, 2 fl. oz (59 ml) bottle.
Summary
The FDA issued a Class II for Energique Mineral Magic Dietary Supplement, 2 fl. oz (59 ml) bottle. by Grato Holdings, Inc.. Reason: Potential microbial contamination (yeast and/or mold)..
Details
Source
Food Recall
External ID
F-1458-2024
Action Date
2024-07-10
Status
Terminated
Category
food
Product Description
Energique Mineral Magic Dietary Supplement, 2 fl. oz (59 ml) bottle.
Lot/Code Info: Lot: G11602 MFD: 06/21; Lot G11747 MFD: 07/22; Lot: G11723 MFD 08/22
Quantity Affected: 1912 bottles
Reason for Recall
Potential microbial contamination (yeast and/or mold).
Distribution
Nationwide US and Canada
Type: Voluntary: Firm initiated
Recall Initiated: 2024-05-03
Company
Woodbine, IA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 51 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Grato Holdings, Inc. has 7 FDA actions in our database, including 7 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Grato Holdings, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Grato Holdings, Inc. have FDA actions?
Grato Holdings, Inc. has 7 FDA actions in our database, including 7 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1458-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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