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FDAFDA · Food and drugs·Recall number D-0164-2024

ALLOPURINOL Tablets, USP 300 MG 500 count Tablets per bottle, Rx only, Manufactured By: Dr. Reddy's Laboratories LA LLC, Shreveport, LA 71106. NDC: 55111-730-05

Published January 3, 2024 · Recall initiated: January 26, 2022

Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.

What to do

Voluntary: Firm initiated · Letter

Recall details

Brand
ALLOPURINOL
Manufacturer
CARDINAL HEALTHCARE
Distributor
Nationwide USA
UPC
0355111729013
Lot
Batch L100813
Risk classification
Class II
Area (FDA)
drug
Country
United States

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