B Force Liquid
FDA Recall NDC 43857-0576
FDA Enforcement Report: View Recall Date, Reasons, and Safety Status
Active & Historical Enforcement Reports
The FDA has identified 1 recorded enforcement report(s) associated with B Force (NDC 43857-0576). A significant event, classified as Class III, was initiated on Jun 18, 2021 by Bioactive Nutritional, Inc.. The reported reason for this action was: "Superpotent"
This specific recall has a current status of TERMINATED, indicating that the FDA considers the recall process finished or the product successfully recovered.
This specific recall has a current status of TERMINATED, indicating that the FDA considers the recall process finished or the product successfully recovered.
Reported Recall Events
Class III Terminated
Superpotent
Jun 18, 2021
Jul 21, 2021
1480 bottles
Recall Profile & Regulatory Data
Event ID
88182
Classification
Class III
Enforcement Status
Terminated
Recalling Firm
Grato Holdings, Inc.
Voluntary / Mandated
Voluntary: Firm initiated
Distribution Pattern
FL
Termination Date
Oct 18, 2022
Product Description
B-Force, Homeopathic, 1 Fl Oz (30 mL) bottle, Distributed by: BioActive Nutritional, Inc., Melbourne, FL 32935, NDC 43857-0576-1
Batch or Lot Expiration Information
Lot# Lot: Z61917
Affected Packages Involved in this Recall
43857-0576-1Product
About FDA Recall Enforcement Reports
FDA recall data documents classified recall actions associated with a product. Most recalls are limited to specific lots, batches, or package configurations rather than every unit of a drug.
If a recall is listed for an NDC, review the affected lot information and package details carefully. Patients and healthcare professionals should confirm whether a specific product in hand matches the lot or package information before assuming it is affected.
