Allopurinol Tablets recall
Allopurinol Tablets, USP 300mg, 100 Tablets per bottle, Rx only, Manufactured By: Dr. Reddy's Laboratories LA LLC, Shreveport, LA 71106 USA, NDC…
Why was Allopurinol Tablets recalled?
Presence of foreign substance.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
L2300594
- Product
- Allopurinol Tablets, USP 300mg, 100 Tablets per bottle, Rx only, Manufactured By: Dr. Reddy's Laboratories LA LLC, Shreveport, LA 71106 USA, NDC…
- Recalling firm
- Dr. Reddy's Laboratories, Inc.
- Quantity
- 20,520 units
- Distribution
- IL, MS, OH
- Recall date
- July 10, 2024
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)