Dr. Reddy's Laboratories recalls 300mg allopurinol tablets for foreign substance presence. Rx-only medication with NDC 55111-730-01. No remedy specified in official notice.
Presence of foreign substance.
Dr. Reddy's recalls 300mg allopurinol tablets (Rx-only) due to foreign substance presence. This affects patients using the medication as prescribed. The recall has no specified remedy in the official notice.
The presence of a foreign substance could cause harm if ingested. However, the official notice does not specify the exact risk level or potential injury.
Patients prescribed allopurinol tablets by a healthcare provider. Those using the medication as directed are most at risk.
Check for the product name 'Allopurinol Tablets, USP 300mg, 100 Tablets per bottle' with NDC 55111-730-01. The medication is prescription-only and manufactured by Dr. Reddy's Laboratories LA LLC in Shreveport, LA.
Verify the product name and NDC number (55111-730-01) to confirm if it's affected.
The official notice does not specify any remedy.
Allopurinol Tablets, USP 300mg, 100 Tablets per bottle (Rx only).
Shreveport, LA 71106 USA by Dr. Reddy's Laboratories LA LLC.
We’ve drafted a message you can send Dr. Reddy's to request your refund or repair — edit it as you like.
Subject: Recall D-0583-2024 — Dr. Reddy's Dr. Reddy's Hello, I own a Dr. Reddy's that is covered by recall D-0583-2024 from Dr. Reddy's. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
