CLASS III Drug recall · Reported 15 Nov 2023 · FDA Enforcement Report
V-force Homeopathic recalled by Grato Holdings
Grato Holdings is recalling V-force Homeopathic per, distributed in Florida. The recall was initiated on 30 Oct 2023 and the FDA has classified it as Class III.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0099-2024
- FDA event ID
- 93354
- Recalling firm
- Grato Holdings, Woodbine, IA
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- 30 Oct 2023
- FDA classified
- 9 Nov 2023
- Reported
- 15 Nov 2023
- Type
- Voluntary: Firm initiated
- Customers notified by
- Telephone
- Reason category
- Packaging Defects
Timeline
| 30 Oct 2023 | Recall initiated by company | |
| 9 Nov 2023 | Classified by FDA | +10 days |
| 15 Nov 2023 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
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).
Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.
Product as listed by the FDA
V-FORCE Homeopathic, 1 FL OZ (30 ml) per glass bottle, Distributed by: BioActive Nutritional, Inc., 1803 N. Wickham Rd., Melbourne, FL 32935
Where it was distributed
Distributed to one direct account in Florida with possible further distribution out of state.
Questions about this recall
Why was it recalled?
Incorrect Product Formulation: product contains Active Ingredient Glandula Suprarenalis Suis 8X instead of Glandula Suprarenalis Bovine 8X (as stated on the product label).
Which lots are affected?
Lot: Z65842 no exp date on product
Where was it sold?
Distributed to one direct account in Florida with possible further distribution out of state.
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class III mean?
Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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