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The United States: Beaumont Bio Med, Inc. issues voluntary nationwide recall of all their homeopathic aqueous/alcohol-based medicines due to the nationwide recall by the contract manufacturer, King Bio, of all their aqueous-based products due to possible microbial contamination (English Only)
 
The US Food and Drug Administration (FDA) announces that Beaumont Bio Med, Inc. is voluntarily recalling its entire aqueous/alcohol-based product line for human use, within expiry, to the consumer level. All products manufactured by the contract manufacturer, King Bio, have been recalled due to possible microbial contamination. For details of the affected products, please refer to the FDA website.

The 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. To date, Beaumont Bio Med has not received any reports of adverse events related to this recall.

Please refer to the following website in FDA for details: http://www.fda.gov/Safety/Recalls/ucm619587.htm

In Hong Kong, the above products are not registered pharmaceutical products. Related news was previously issued by FDA, and was posted on the Drug Office website on 21 Jul 2018, 23 Aug 2018, 29 Aug 2018 and 30 Aug 2018.

Ends/Friday, Sep 7, 2018
Issued at HKT 16:00
 
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