Approximately 141,015 vials of Ivermectin Liquid for Horses (10 mg per mL) have been recalled because a precipitate or sediment forms in the bottle after it has been opened. This recall affects 100-ml and 200-ml multi-dose vials sold under the brand names Phoenectin, Butler Parid EQ, Ivercide, and ProMectin E. Because the medication may not be uniform after opening, horses may receive an incorrect dose, which could lead to ineffective treatment of parasites. Owners should consult their veterinarian or pharmacist regarding any used or unused vials from the affected brands.
The formation of a precipitate means the active medication is no longer properly dissolved in the liquid, which can result in the animal receiving too much or too little ivermectin. This lack of dose uniformity can lead to treatment failure or potential toxicity depending on the concentration of the sediment.
Refund or credit through pharmacy or veterinarian
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