Recalls / Class III
Class IIID-0653-2021
Product
B-Force, Homeopathic, 1 Fl Oz (30 mL) bottle, Distributed by: BioActive Nutritional, Inc., Melbourne, FL 32935, NDC 43857-0576-1
- Brand name
- B Force
- Generic name
- 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
- Active ingredients
- Arsenic Trioxide, Atropa Belladonna, Botulinum Toxin Type A, Clostridium Perfringens, Echinacea Angustifolia Whole, Escherichia Coli, Goldenseal, Handroanthus Impetiginosus Bark, Hypericum Perforatum Whole, Lomatium Dissectum Root, Myrrh, Nasturtium Officinale, Phosphorus, Propolis Wax, Proteus Morganii, Proteus Vulgaris, Pseudomonas Aeruginosa, Salmonella Enterica Subsp. Enterica Serovar Typhi, Sus Scrofa Adrenal Gland, Sus Scrofa Lymph, Sus Scrofa Spleen, Sus Scrofa Thymus, Sus Scrofa Thyroid
- Route
- Oral
- NDC
- 43857-0576
- Affected lot / code info
- Lot: Z61917
Why it was recalled
Superpotent
Recalling firm
- Firm
- Grato Holdings, Inc.
- Manufacturer
- BioActive Nutritional, Inc.
- Notification channel
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Type
- Voluntary: Firm initiated
- Address
- 201 Apple Blvd, Woodbine, Iowa 51579-1503
Distribution
- Quantity
- 1480 bottles
- Distribution pattern
- FL
Timeline
- Recall initiated
- 2021-06-18
- FDA classified
- 2021-07-12
- Posted by FDA
- 2021-07-21
- Terminated
- 2022-10-18
- Status
- Terminated
Source: openFDA Drug Enforcement endpoint. Recall record D-0653-2021. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.