Grato Holdings, Inc.

Complete recall history across all FDA and CPSC categories — 20 total recalls

Grato Holdings, Inc. appears in recall records across 2 categories. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Food Recalls (6)

FDA food safety enforcement actions by Grato Holdings, Inc.

Date Product Reason Class
May 3, 2024 BioActive Nutritional MINAPLEX, Botanical Herbal Supplement; 1 Fl. oz. (30 ml... Potential microbial contamination (yeast and/or mold). Class II
May 3, 2024 Energique Mineral Magic Dietary Supplement, 2 fl. oz (59 ml) bottle. Potential microbial contamination (yeast and/or mold). Class II
Apr 16, 2018 Energique, Dietary Supplement, Enervimin CNCR Focus, Dist. by Energique Inc.... Multiple products marketed as dietary supplements are unapproved new drugs ba... Class II
Apr 16, 2018 Peaceful Mountain -Stomach Rescue - Dietary supplement - Elemental silver (45... Multiple products marketed as dietary supplements are unapproved new drugs ba... Class II
Apr 16, 2018 Peaceful Mountain, Nasal Rescue, Dietary Supplement, Natural Sinus Support, D... Multiple products marketed as dietary supplements are unapproved new drugs ba... Class II
Apr 16, 2018 Energique, Herbal Supplement, Octocom,; Dist. by Energique, Inc. Woodbine, IA... Multiple products marketed as dietary supplements are unapproved new drugs ba... Class II

Drug Recalls (14)

FDA drug safety enforcement actions by Grato Holdings, Inc.

Date Product Reason Class
Oct 30, 2023 V-FORCE Homeopathic, 1 FL OZ (30 ml) per glass bottle, Distributed by: BioAc... Incorrect Product Formulation: product contains Active Ingredient Glandula Su... Class III
May 24, 2022 Earache Drops, 0.33 FL OZ (10 mL) bottles, Distributed by: Walgreen Co., 200 ... Microbial contamination of non-sterile product. Class II
May 24, 2022 Homeopathic EarAche Ear Drops, 0.33 FL OZ (10 mL) bottles, Distributed by: CV... Microbial contamination of non-sterile product. Class II
May 24, 2022 Homeopathic EarAche Drops, 0.33 FL OZ (10 mL) bottles, Distributed by: RITE A... Microbial contamination of non-sterile product. Class II
Jun 18, 2021 B-Force, Homeopathic, 1 Fl Oz (30 mL) bottle, Distributed by: BioActive Nutri... Superpotent Class III
Sep 17, 2020 Homeopathic Energy Catalyst, 1 fl oz (30 mL) Distributed by: Deseret Biologic... Labeling: Product Contains Undeclared API; Incorrect formulation Class III
Jul 16, 2020 HGH Vitality Homeopathic, 90 tablets, NDC 43742-1299-1, Dist. by Deseret Biol... Labeling: Error on Declared Strength Class II
Nov 15, 2019 Colostat, Homeopathic Remedy, 1 fl. oz. (30 mL) per bottle, 20% Ethanol, Dist... Labeling mix-up - Indications on product label are incorrect. Class III
Dec 22, 2015 Energique, Homeopathic Remedy, Joint Pain & Stiffness Relief, Topical Spray, ... Microbial Contamination of Non Sterile Products; testing revealed out of spec... Class II
Dec 22, 2015 Energique, Homeopathic Remedy, First Aid Pain & Trauma Relief, 1 fl oz (30 ml... Microbial Contamination of Non Sterile Products; testing revealed out of spec... Class II
Dec 22, 2015 Energique, Homeopathic Remedy, Headache Pain & Sinus Pressure Relief, Topical... Microbial Contamination of Non Sterile Products; testing revealed out of spec... Class II
Dec 22, 2015 Energique, Homeopathic Remedy, Shingles Pain & Ulceration Relief, Topical Spr... Microbial Contamination of Non Sterile Products; testing revealed out of spec... Class II
Dec 22, 2015 Energique, Homeopathic Remedy, Muscle/Tendon Pain & Stress Relief, Topical Sp... Microbial Contamination of Non Sterile Products; testing revealed out of spec... Class II
Dec 22, 2015 Energique, Homeopathic Remedy, Skin Irritant & Healing Support, Topical Spray... Microbial Contamination of Non Sterile Products; testing revealed out of spec... Class II

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

Yes. You can search for any company using the firm/manufacturer pages for each category: Food Firms, Drug Firms, Device Firms, or Product Manufacturers. You can also use the search functionality on any browse page to find recalls by company name.

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