Spirit Pharmaceuticals, LLC is recalling 144 bottles of Ibuprofen Tablets USP (200 mg) sold in 100-count bottles. This over-the-counter pain reliever and fever reducer is being recalled because it was manufactured under conditions that deviated from Current Good Manufacturing Practice (CGMP) standards, which were identified following a previous recall. Consumers should contact their healthcare provider or pharmacist regarding the use of this medication and for instructions on returning any remaining product.
Manufacturing deviations mean the safety, quality, and purity of the medication cannot be guaranteed. While no specific injuries or adverse events have been reported for this lot, drugs produced outside of established safety standards may not contain the correct amount of active ingredient or could contain unintended impurities.
Manufacturer-initiated drug recall refund and guidance
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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