Unrated Drug recall · FDA · Published September 17, 2020

Grato Holdings Homeopathic Energy Catalyst Recall: Undeclared API in Product

Grato Holdings recalls Homeopathic Energy Catalyst 1 fl oz (30 mL) due to undeclared active ingredients and incorrect formulation. Consumers should check product labels for lot numbers Z60852 or Z60012.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #D-0099-2021Drug Grato Holdings ›

Recall notice

Labeling: Product Contains Undeclared API; Incorrect formulation

Take action

Contact the company

Recalling firmGrato Holdings, Inc.201 Apple Blvd · Woodbine, IA 51579-1503

✎ GovInfoNow plain-language explainer

Grato Holdings is recalling Homeopathic Energy Catalyst 1 fl oz (30 mL) because it contains undeclared active ingredients and has an incorrect formulation. This could lead to improper use or health risks if the product is consumed without knowing its true composition. Read more at govinfonow.com/recall/36768-grato-holdings-homeopathic-energy-catalyst-recall-undeclared-api-in-product.

Source Summary by GovInfoNow · govinfonow.com/recall/36768-grato-holdings-homeopathic-energy-catalyst-recall-undeclared-api-in-product · Updated October 4, 2026 · FDA enforcement record: FDA #D-0099-2021

Cite this page

“Grato Holdings Homeopathic Energy Catalyst Recall: Undeclared API in Product.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/36768-grato-holdings-homeopathic-energy-catalyst-recall-undeclared-api-in-product. Based on FDA recall #D-0099-2021 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0099-2021%22&limit=1).

The FDA announced on 2020-09-17 that Grato Holdings, Inc. voluntarily recalled Homeopathic Energy Catalyst due to labeling errors containing undeclared active pharmaceutical ingredients and incorrect formulation. The recall affects 399 bottles distributed in Utah.

How to tell if you have it

Brand: Grato Holdings
Product: Homeopathic Energy Catalyst, 1 fl oz (30 mL)
Distributed by: Deseret Biologicals, Inc., 469 W. Parkland Drive Sandy, UT 84070
NDC: 43742-0756-1
Lot codes: Z60852, Z60012

The hazard

The product contains undeclared active pharmaceutical ingredients and has an incorrect formulation. The FDA classified this as a Class III recall.

Context

GovInfoNow's records show Grato Holdings, Inc. has had 8 other recalls on record since 2015-12-22. Other recent recalls of similar products include BioActive Nutritional MINAPLEX Herbal Supplement Recall (2024-05-03), Grato Holdings V-FORCE Homeopathic Recall (2023-10-30), and Grato Holdings Homeopathic Ear Drops Recall (2022-05-24). Other recent recalls of similar products include Gasco Isopropyl Alcohol 70% Recall (2026-05-29), Haleon Gas-X Extra Strength Softgels Recall (2026-06-04), and Graviti Furosemide Tablets Recall (2026-01-10).

How to tell if you have this one

Check the label for the product name 'Homeopathic Energy Catalyst', 1 fl oz (30 mL), and lot numbers Z60852 or Z60012. The product was distributed by Deseret Biologicals, Inc. in Sandy, UT.

Brand
Grato Holdings
Category
Drug

Based on the official FDA remedy

What to do — step by step

Check Product Label
Look for lot numbers Z60852 or Z60012 on the label to confirm if the product is recalled.

Where it went and when

Where it was distributed

Distributed in Utah.

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

States: Utah.

Recall timeline

FDA terminated this recall 2.1 years after the firm started it.

Sep 17, 2020Firm started the recall
Nov 19, 2020FDA classified it Class III
Nov 25, 2020Published in FDA’s Enforcement Report
Oct 18, 2022FDA terminated the recall

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

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Keep exploring

Link to this recall

<a href="https://govinfonow.com/recall/36768-grato-holdings-homeopathic-energy-catalyst-recall-undeclared-api-in-product">Grato Holdings Homeopathic Energy Catalyst Recall: Undeclared API in Product (GovInfoNow)</a>

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 #D-0099-2021 (September 17, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0099-2021 to see it in context.
Plain-language summary written by qwen3:4b on October 4, 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.