Class III · Low risk
V-FORCE Homeopathic
Incorrect Product Formulation: product contains Active Ingredient Glandula Suprarenalis Suis 8X instead of Glandula Suprarenalis Bovine 8X (as stated on the product label).
B-Force
Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
Why it was recalled
Superpotent
Cause type: Wrong potency / content
Sub- or super-potent product, or a failed content-uniformity / assay test. You may receive too little or too much active ingredient - a direct dosing risk. All wrong potency / content recalls.
What was recalled
B-Force, Homeopathic, 1 Fl Oz (30 mL) bottle, Distributed by: BioActive Nutritional, Inc., Melbourne, FL 32935, NDC 43857-0576-1
Affected NDC
43857-0576-01
Compare with the code on your package — it is the most precise check available.
Product details
From the FDA NDC directory, for the product code this recall names. Compare with the label on your package.
| Product | Strength | Form & route | Labeler | Type |
|---|---|---|---|---|
| B Force Echinacea Angustifolia, Lomatium Dissectum, Myrrha, Nasturtium Aquaticum, Tabebuia Impetiginosa, Hydrastis Canadensis, Propolis, Glandula Suprarenalis Suis, Lymph Node (Suis), Spleen (Suis), Thymus (Suis), Thyroidinum (Suis), Arsenicum Album, Belladonna, Hypericum Perforatum, Phosphorus, Botulinum, Colibacillinum Cum Natrum Muriaticum, Proteus (Vulgaris), Pseudomonas Aeruginosa, Proteus (Morgani), Salmonella Typhi Nosode, Clostridium Perfringens NDC 43857-0576 |
ECHINACEA ANGUSTIFOLIA WHOLE 3 [hp_X]/mL; LOMATIUM DISSECTUM ROOT 3 [hp_X]/mL; MYRRH 3 [hp_X]/mL; NASTURTIUM OFFICINALE 3 [hp_X]/mL; HANDROANTHUS IMPETIGINOSUS BARK 3 [hp_X]/mL; GOLDENSEAL 5 [hp_X]/mL; PROPOLIS WAX 6 [hp_X]/mL; SUS SCROFA ADRENAL GLAND 8 [hp_X]/mL; SUS SCROFA LYMPH 8 [hp_X]/mL; SUS SCROFA SPLEEN 8 [hp_X]/mL; SUS SCROFA THYMUS 8 [hp_X]/mL; SUS SCROFA THYROID 8 [hp_X]/mL; ARSENIC TRIOXIDE 12 [hp_X]/mL; ATROPA BELLADONNA 12 [hp_X]/mL; HYPERICUM PERFORATUM WHOLE 12 [hp_X]/mL; PHOSPHORUS 12 [hp_X]/mL; BOTULINUM TOXIN TYPE A 30 [hp_X]/mL; ESCHERICHIA COLI 30 [hp_X]/mL; PROTEUS VULGARIS 30 [hp_X]/mL; PSEUDOMONAS AERUGINOSA 30 [hp_X]/mL; PROTEUS MORGANII 30 [hp_X]/mL; SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR TYPHI 33 [hp_X]/mL; CLOSTRIDIUM PERFRINGENS 15 [hp_C]/mL | Liquid Oral |
BioActive Nutritional, Inc. | OTC |
- Recalling firm
- Grato Holdings, Inc.
- NDC code
- 43857-0576-1
- Origin
- IA, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-0653-2021 · FDA notice
Low risk, still worth a check. Class III means the product is unlikely to cause harm but breaks an FDA rule (often labeling). If your lot matches, your pharmacy will normally swap it; there is no need for alarm. This recall is now terminated, which means the firm has finished removing the affected product; anything on pharmacy shelves today should be unaffected.
Other recalls by Grato Holdings, Inc.
All 2021 recalls
Class II · Moderate risk
Earache Drops
Microbial contamination of non-sterile product.
Class II · Moderate risk
Homeopathic EarAche Ear Drops
Microbial contamination of non-sterile product.
Class II · Moderate risk
Homeopathic EarAche Drops
Microbial contamination of non-sterile product.
Other wrong potency / content recalls from 2021
All wrong potency / content recalls
Class II · Moderate risk
Pioglitazone Tablets USP
Superpotent and Failed Tablet/Capsule Specifications
Class II · Moderate risk
Penicillin V Potassium for Oral Solution
Subpotent
Class III · Low risk
CTx12 5000 Kit which contains 3 boxes of CariFree CTx4 GEl 5000…
Subpotent Drug: Product contains less Sodium Fluoride than listed on product label.
Class III · Low risk
CariFree sample boxes
Subpotent Drug: Product contains less Sodium Fluoride than listed on product label.
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