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Class II · ModerateRecall completed

Allopurinol

Could cause temporary or reversible harm; serious harm is unlikely.

Does this affect you?
Check your lot numberL2300594
Where it was soldIL, MS, OH
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

Presence of foreign substance.

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byDr. Reddy's Laboratories LA LLC, Shreveport, LA 71106 USA
Brand nameALLOPURINOL
Generic nameALLOPURINOL
Active ingredient(s)ALLOPURINOL
Distributed by / forDr. Reddy's Laboratories, Inc.
NDC55111-730-01
Show the full FDA record
Full product labelAllopurinol 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.
Recalling firmDr. Reddy's Laboratories, Inc.
DistributionIL, MS, OH
Quantity20,520 units
Recall initiated2024-06-07
Report date2024-07-10
Recall completed2025-12-22
Recall numberD-0583-2024
ClassificationClass II
FDA statusTerminated
Origin on filePrinceton NJ United States

Related

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Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.