V-FORCE Homeopathic — Class III drug recall D-0099-2024
Terminated recall by Grato Holdings, Inc., reported 2023-11-15, distributed in FL. Incorrect Product Formulation: product contains Active Ingredient Glandula Suprarenalis Suis 8X instead of Gla
| Recall number | D-0099-2024 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Grato Holdings, Inc., Woodbine, IA, United States |
| Recall initiated | 2023-10-30 |
| Classified | 2023-11-09 |
| Reported by FDA | 2023-11-15 |
| Terminated | 2024-05-12 |
| Distributed | FL |
| Quantity | 1,333 |
| Reason classes | labeling |
| Lot numbers | Z65842 |
Product
V-FORCE Homeopathic, 1 FL OZ (30 ml) per glass bottle, Distributed by: BioActive Nutritional, Inc., 1803 N. Wickham Rd., Melbourne, FL 32935
Reason for recall
Incorrect Product Formulation: product contains Active Ingredient Glandula Suprarenalis Suis 8X instead of Glandula Suprarenalis Bovine 8X (as stated on the product label).
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0099-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.