Wal-Fex D Fexofenadine HCl 60 mg/ Pseudoephedrine HCl recall: Impurity Out of Spec
Wal-Fex D Fexofenadine HCl 60 mg/ Pseudoephedrine HCl 120 mg, Extended-Release Tablets, USP, Allergy & Congestion, 20-count box.Distributed by…
Why was Wal-Fex D Fexofenadine HCl 60 mg/ Pseudoephedrine HCl recalled?
Testing of Fexofenadine HCl and Pseudoephedrine Failed Impurities/Degradation Specifications: elevated substance results that were reported above or near the specification limit
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 GKT0406, EXP 3/2020
- Product
- Wal-Fex D Fexofenadine HCl 60 mg/ Pseudoephedrine HCl 120 mg, Extended-Release Tablets, USP, Allergy & Congestion, 20-count box.Distributed by…
- Recalling firm
- Sun Pharmaceutical Industries, Inc.
- Quantity
- 17,904 20-count units
- Distribution
- Nationwide in the USA
- Recall date
- June 26, 2019
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)