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Dr. Reddy's Laboratories, Inc. — Allopurinol Tablets, USP 300mg, 100 Tablets per bottle, Rx only
Do not stop taking this without speaking to your pharmacist or doctor.
What’s wrong
Presence of foreign substance.
The Recall Registry rates this serious — FDA Class II: temporary or medically reversible health harm.
What to do
Check the lot numbers below against what you have. Do not stop taking a prescription medicine because of a recall without speaking to your pharmacist or doctor first — for many medicines stopping is more harmful than continuing, and they can tell you whether yours is affected and what to do about it.
Who to contact: Recalling firm: Dr. Reddy's Laboratories, Inc.
The product
Allopurinol Tablets, USP 300mg, 100 Tablets per bottle, Rx only, Manufactured By: Dr. Reddy's Laboratories LA LLC, Shreveport, LA 71106 USA, NDC 55111-730-01.
Details
- Units affected
- 20,520 units
- Recall date
- June 7, 2024
- Brand
- Dr. Reddy's Laboratories, Inc.
IL, MS, OH
The official notice
This recall was issued by the U.S. Food and Drug Administration. The Recall Registry summarises it — always confirm the details at the source.
Their exact wording: “Dr. Reddy's Laboratories, Inc. — Allopurinol Tablets, USP 300mg, 100 Tablets per bottle, Rx only, Manufactured By: Dr. Reddy's Laboratories LA LLC, Shreveport, LA 71106 USA, NDC 55111-730-01.”
Worried about the other things in your house? You can write down what you have and be told if one is recalled — or, if you sell second-hand, check your whole stock at once.
Filed under: Prescription medicine