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

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: Silver Star Brand’s voluntary recall of homeopathic drug products HelloLife’s voluntary recall of drug products labeled as homeopathic ; Beaumont Bio Med’s voluntary recall of all water- and alcohol-based products; and BioLyte Laboratories voluntary recall of NeoRelief Health care professionals and patients should report any adverse events associated with Sprayology’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. For more information, please visit: Sprayology Recall.