FDAFDA · Food and drugs·Recall number D-1873-2019
Wal-Fex (Fexofenadine Hydrochloride) Tablets USP, 180 mg, 5-count cartons, Distributed By: Walgreen Co., 200 Wilmot Rd., Deerfield, IL 60015, NDC 0363-0097-55.
Published September 25, 2019 · Recall initiated: August 23, 2019
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
Failed Impurities/Degradation Specifications
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Aurolife Pharma, LLC
- Distributor
- Nationwide in the USA
- Lot
- Lot #: 06718027A1, Exp 09/21
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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