Silver Star Brands, Inc. has voluntarily recalled two PetAlive® products for pets. The products, PetAlive Plump-Up Pet Oral Spray and PetAlive Allergy Itch Ease Oral Spray, have been found to contain microbial contamination. 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 and animals. To date, Silver Star Brands, Inc. has not received any reports of adverse events related to this recall.

These products can be identified by the main label on the bottle and the lot number that is printed on the label. Each product recalled is an individual 2-oz. oral spray in amber bottles, and was manufactured at the King Bio, Inc. facility in Asheville, NC. The products were distributed nationwide via wholesale, retail and online sales.

Product	NDC		UPC	Lot	Expiration Date
PetAlive Plump-Up Pet Oral Spray	68703-290-02		818837013908	K011617E	01/20
PetAlive Allergy Itch Ease Oral Spray	68703-135-59		818837011102	K111617B	11/20

Consumers should discontinue use of these products and contact Silver Star Brands, Inc. at Nativeremedies@silverstarbrands.com to make arrangements to return the product. Consumers with questions regarding this recall can contact Silver Star Brands, Inc. at 1-888- 736-6389 Monday – Friday 8:00 am – 5:00 pm CST or email Nativeremedies@silverstarbrands.com. Consumers should contact their veterinarian if they believe their pets have experienced any problems that may be related to using these products.

Adverse reactions or quality problems associated with the use of this product may be reported to FDA’s MedWatch Adverse Event Reporting program online at www.fda.gov/medwatch/report.htm or by mail by downloading and mailing the form found at www.fda.gov/MedWatch/getforms.htm. Consumers can also call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178.

Click here to see the full FDA recall notice.