Approximately 985,411 vials of Ketamine Hydrochloride Injection and Butorphanol Tartrate Injection are being recalled because they were not manufactured in compliance with safety standards. There has also been an increased trend in serious adverse events reported in animals associated with the use of these products. These veterinary medications were sold nationwide and internationally under various brand names including AmTech, Butler, LLOYD Laboratories, Phoenix Pharmaceutical, VEDCO, RXVeterinary Products, and Fort Dodge.
Failure to follow good manufacturing practices can lead to contaminated or inconsistent medication doses, while the increase in serious adverse events suggests the products may cause unexpected or severe medical complications in treated animals.
Drug recall baseline remedy
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.
AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.
Sources: FDA iRES · Raw API Response