Grato Holdings, Inc.
Complete recall history across all FDA and CPSC categories — 20 total recalls
Recall Summary
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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