Allergy Relief D Fexofenadine HCl recall: Failed Dissolution
Allergy Relief D Fexofenadine HCl, 60 mg I Pseudoephedrine HCl, 120 mg, Extended Release Tablets, USP, 30 Extended-Release Tablets USP, Distributed By Walmart Inc., Bentonville, AR 72716, Product of India, NDC 49035-273-30.
Why was Allergy Relief D Fexofenadine HCl recalled?
Failed dissolution specifications
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?
Lot #: AC2103329B
- Product
- Allergy Relief D Fexofenadine HCl, 60 mg I Pseudoephedrine HCl, 120 mg, Extended Release Tablets, USP, 30 Extended-Release Tablets USP, Distributed By Walmart Inc., Bentonville, AR 72716, Product of India, NDC 49035-273-30.
- Recalling firm
- Dr. Reddy's Laboratories, Inc.
- Quantity
- 9,984 cartons
- Distribution
- USA Nationwide.
- Recall date
- December 15, 2021
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)