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FDA alerts consumers of Sprayology’s voluntary nationwide recall of homeopathic water-based medicines due to microbial contamination

FDA alerts consumers of Sprayology’s voluntary nationwide recall of homeopathic water-based medicines due to microbial contamination

[10/11/2018] The Food and Drug Administration is alerting consumers about a voluntary recall of all lots with expiration dates from October 2018 to July 2022 of Sprayology’s water-based homeopathic product line for human use. These products are labeled as a homeopathic and are being recalled due to microbial contamination at the King Bio Inc. manufacturing facility in Asheville, North Carolina.

Administration or use of drug products with microbial contamination could potentially result in increased infections that may require medical intervention.

Previously, FDA alerted consumers to four other voluntary recalls related to King Bio’s recall:

Health care professionals and patients should report any adverse events associated with Sprayology's products to the FDA’s MedWatch Adverse Event Reporting program:

Health care professionals and patients should report any adverse events associated with Sprayology's products to the FDA’s MedWatch Adverse Event Reporting program: