Dr. Reddy's Laboratories, Inc. is recalling 20,520 units of Allopurinol (allopurinol) Tablets, USP 300mg, because of the presence of a foreign substance. The recalled medication was distributed in 100-count bottles to pharmacies in Illinois, Mississippi, and Ohio. Consumers who have this prescription should consult their pharmacist or healthcare provider regarding their treatment.
The presence of an unidentified foreign substance in medication can cause physical irritation or unexpected health reactions if ingested. No specific injuries or adverse events have been reported in the recall notice.
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Manufactured By: Dr. Reddy's Laboratories LA LLC, Shreveport, LA 71106 USA
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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