Ascent Pharmaceuticals is recalling 9,768 bottles of Hydrocodone Bitartrate and Acetaminophen (10mg/325mg) because a bottle was found to contain a different medication, Losartan Potassium (100 mg). This recall affects 100-count bottles of the prescription pain reliever manufactured for Camber Pharmaceuticals. Consumers should contact their healthcare provider or pharmacist immediately to determine if their medication is affected. Return any unused tablets to the pharmacy for a refund and contact the manufacturer for further instructions.
Taking an incorrect medication like Losartan Potassium (a blood pressure drug) instead of the intended Hydrocodone pain reliever could lead to unintended side effects or lack of pain management. There is a risk of dangerous drug interactions or severe health consequences if the wrong medication is consumed.
Healthcare provider consultation and pharmacy refund
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
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