sábado, 8 de septiembre de 2018

FDA is alerting consumers of Beaumont Bio Med’s voluntary recall of all water- and alcohol-based products - Drug Information Update



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.

For more information please visit: King Bio

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