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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Low RiskFDA Drug
Medications & Supplements/Dietary Supplements

Grato Holdings, Inc.: Homeopathic Energy Catalyst Recalled for Undeclared Ingredient and Label Error

Agency Publication Date: November 18, 2020
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Summary

Approximately 399 bottles of Homeopathic Energy Catalyst (1 fl oz / 30 mL) have been recalled because the product contains an undeclared active pharmaceutical ingredient (API) and was manufactured with an incorrect formulation. The label does not accurately reflect the contents of the medication, which could lead to unintended drug exposure or improper treatment. These products were distributed by Deseret Biologicals, Inc. specifically within Utah and involve two specific lot numbers.

Risk

The presence of an undeclared active ingredient means consumers may unknowingly ingest substances that could interact with other medications or cause adverse health effects. An incorrect formulation further poses a risk as the product may not perform as intended or may contain ingredients at levels not specified on the packaging.

What You Should Do

  1. Check your bottle of Homeopathic Energy Catalyst (1 fl oz / 30 mL) for lot numbers Z60852 or Z60012 and NDC 43742-0756-1.
  2. Immediately stop using the affected product if your bottle matches the recalled lot numbers.
  3. Contact your healthcare provider or pharmacist to discuss any health concerns or to find a suitable replacement for this homeopathic product.
  4. Return any unused product to the place of purchase or the pharmacy where it was obtained for a full refund.
  5. Contact Grato Holdings, Inc. at 201 Apple Blvd, Woodbine, Iowa for further instructions regarding the return or disposal of the product.
  6. For additional questions or to report a problem, contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls.

Your Remedy Options

๐Ÿ’ฐFull Refund

Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

Affected Products

Product: Homeopathic Energy Catalyst (1 fl oz / 30 mL)
Model:
NDC 43742-0756-1
Lot Numbers:
Z60852
Z60012

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 86690
Status: Resolved
Manufacturer: Grato Holdings, Inc.
Sold By: Deseret Biologicals, Inc.
Manufactured In: United States
Units Affected: 399 bottles
Distributed To: Utah
Agency Last Updated: November 19, 2020

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.