Grato Holdings V-FORCE Homeopathic Recall: Incorrect Active Ingredient
Grato Holdings recalls V-FORCE Homeopathic 1 fl oz bottles due to incorrect active ingredient formulation. Product contains Glandula Suprarenalis Suis 8X instead of G: Glandula Suprarenalis Bovine 8X as labeled.
Lower-risk recall
Incorrect Product Formulation: product contains Active Ingredient Glandula Suprarenalis Suis 8X instead of Glandula Suprarenalis Bovine 8X (as stated on the product label).
Contact the company
What happened, in plain English
Grato Holdings is recalling V-FORCE Homeopathic 1 fl oz bottles because they contain the wrong active ingredient (pig adrenal extract instead of cow adrenal extract) as labeled. This could lead to ineffective treatment if used for medical purposes. Read more at govinfonow.com/recall/33027-grato-holdings-v-force-homeopathic-recall-incorrect-active-ingredient.
Source Summary by GovInfoNow · govinfonow.com/recall/33027-grato-holdings-v-force-homeopathic-recall-incorrect-active-ingredient · Updated September 23, 2026 · FDA enforcement record: FDA #D-0099-2024
Cite this page
“Grato Holdings V-FORCE Homeopathic Recall: Incorrect Active Ingredient.” GovInfoNow, updated September 23, 2026. https://govinfonow.com/recall/33027-grato-holdings-v-force-homeopathic-recall-incorrect-active-ingredient. Based on FDA recall #D-0099-2024 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0099-2024%22&limit=1).
Why it’s dangerous
The product contains Glandula Suprarenalis Suis 8X (pig adrenal extract) instead of Glandula Suprarenalis Bovine 8X (cow adrenal extract) as labeled. This incorrect formulation may result in ineffective treatment for intended medical uses.
Who’s affected
People who own or use V-FORCE Homeopathic 1 fl oz bottles distributed by BioActive Nutritional, Inc. in Melbourne, FL. Those using the product for medical purposes may be at higher risk due to incorrect formulation.
How to tell if you have this one
Check for V-FORCE Homeopathic 1 fl oz (30 ml) glass bottles with lot number Z65842 distributed by BioActive Nutritional, Inc. in Melbourne, FL.
- Brand
Grato Holdings- Category
Drug
What to do — step by step
Check Product Label
Verify the product label for the lot number Z65842 and the manufacturer's distribution details.
Where it went and when
Where it was distributed
Distributed in Florida.
FDA distribution: “Distributed to one direct account in Florida with possible further distribution out of state.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Florida.
Recall timeline
FDA terminated this recall 6 months after the firm started it.
- Firm started the recall
- FDA classified it Class III
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Similar recalls
Latest drug recalls
Keep exploring
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-0099-2024 (October 30, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0099-2024 to see it in context.
- Plain-language summary written by qwen3:4b on September 23, 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.