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Drug FDA Class II Terminated Foreign material

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.

Dr. Reddy's Laboratories, Inc. Published Jul 10, 2024

Risk level

Class II

May cause a temporary or reversible health problem; slight chance of serious harm.

Severity score 45/100

What should you do?

  • Check whether you have this product, using the lot codes, UPCs, and dates listed below.
  • Do not eat, serve, or sell the affected product.
  • Return it to the place of purchase for a refund, or throw it away in a sealed bag so people and animals can’t get to it.
  • Contact Dr. Reddy's Laboratories, Inc. or your place of purchase with questions, and see the source record below for full details.
Reason for recall

Presence of foreign substance.

Hazards

Foreign Substance · primary

Affected products (1)

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.

ALLOPURINOL · 20,520 units

NDC: 55111-729, 55111-730, 55111-729-01, 55111-729-10, 55111-730-01, 55111-730-05
Code info: L2300594

Affected areas

IllinoisMississippiOhio

Timeline

  1. Initiated
    Jun 7, 2024
  2. Published
    Jul 10, 2024
  3. Terminated
    Dec 22, 2025
Recall number
D-0583-2024
Agency
U.S. Food and Drug Administration
Country
US
Source data (openFDA JSON) About FDA enforcement reports

FDA records come from the openFDA drug enforcement-report dataset — the agency's full weekly enforcement list. Most entries are not issued as consumer press releases, so they won't appear on fda.gov/recalls or in a web search. The source record link above resolves this exact recall by its number.