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Grato Holdings, Inc. Recall: Potential microbial contamination (yeast and/or mold).

United States

TerminatedClass II

Company
Grato Holdings, Inc.
Product
BioActive Nutritional MINAPLEX, Botanical Herbal Supplement;…
Recall date
May 3, 2024
Terminated
July 5, 2024
Source
FDA

Reason for recall

Potential microbial contamination (yeast and/or mold).

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
BioActive Nutritional MINAPLEX, Botanical Herbal Supplement; 1 Fl. oz. (30 ml) bottle. Not published in this source record 261 bottles Lot J28761

Distribution

  • Nationwide US and Canada

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-1459-2024
Event ID
94577
Status
Terminated
Classification
Class II
Company
Grato Holdings, Inc.
Product description
BioActive Nutritional MINAPLEX, Botanical Herbal Supplement; 1 Fl. oz. (30 ml) bottle.
Quantity
261 bottles
Reason
Potential microbial contamination (yeast and/or mold).
Recall initiation date
May 3, 2024
Report date
July 10, 2024
Classification date
Not published in this source record
Termination date
July 5, 2024
Distribution pattern
Nationwide US and Canada
UPC, lot, and code information
Lot J28761
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Other products recalled under this same event

This recall shares FDA event ID 94577 with 1 other product entry in Public Health Trace.

FDA Recall United States Terminated Historical recordClass II

Grato Holdings, Inc.

Product
Energique Mineral Magic Dietary Supplement, 2 fl. oz (59 ml)…
Published
July 10, 2024
Distribution
Nationwide

View recall →

Responsible company: Grato Holdings, Inc.

Other recalls from Grato Holdings, Inc.

FDA Recall United States Terminated Historical recordClass II

Grato Holdings, Inc.

Product
Energique Mineral Magic Dietary Supplement, 2 fl. oz (59 ml)…
Published
July 10, 2024
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

V-FORCE Homeopathic, 1 FL OZ (30 ml) per glass bottle, Distributed by: BioActive Nutritional, Inc., 1803 N. Wickham Rd., Melbourne, FL 32935

by Grato Holdings, Inc.

Published
November 15, 2023
Distribution
Distributed to one direct account in Flo…

View recall →

FDA Recall Terminated Historical recordClass II

Earache Drops, 0.33 FL OZ (10 mL) bottles, Distributed by: Walgreen Co., 200 Wilmot Rd., Deerfield, IL 60015. NDC 0363-3233-15

by Grato Holdings, Inc.

Published
June 15, 2022
Distribution
Nationwide

View recall →

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.