[9/7/2018] The Food and Drug Administration is alerting consumers and health care professionals to a voluntary
recall of all water- and alcohol-based Beaumont Bio Med Inc. (Grand Rapids, Michigan) drug products. These products, labeled as homeopathic, are being recalled due to microbial contamination at the manufacturing facility. 

Administration or use of drug products with microbial contamination could potentially result in increased infections that may require medical intervention, and could result in infections that could be life threatening to certain individuals.

These products were manufactured at the King Bio, Inc. facility in Asheville, North Carolina. Previously, FDA alerted consumers of HelloLife’s voluntary recall of drug products labeled as homeopathic, also manufactured by King Bio.

Health care professionals and patients are encouraged to report any adverse events associated with Beaumont’s drug products to the FDA’s MedWatch Adverse Event Reporting program:

• Complete and submit the report online at www.fda.gov/medwatch/report.htm; or
• Download and complete the form, then submit it via fax at 1-800-FDA-0178.