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Home Prescription medicine Dr. Reddy's Laboratories, Inc. — Allopurinol…

Food & drug recall · FDAJune 7, 2024Serious

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 seriousFDA 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.
Model, lot or SKU numbers
L2300594
Where it was distributed

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.

Read it on FDA

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

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