FDAFDA · Food and drugs·Recall number D-1048-2019
Losartan Potassium Tablets, USP, 25 mg, 30 tablet bottles, Rx Only, Distributed by: Wal-Mart, Bentonville, AR 72716, Manufactured for: Camber Pharmaceuticals, Inc. Piscataway, NJ 08854, Packaged by: Legacy Pharmaceutical Packaging LLC, Earth City, MO 63045 NDC 68645-577-54
Published March 27, 2019 · Recall initiated: March 1, 2019
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
CGMP Deviations: presence of an impurity, N-Methylnitrosobutyric acid (NMBA) detected
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Legacy Pharmaceutical Packaging LLC
- Distributor
- Wal-Mart distribution centers in AR, CA, GA, IN and MD
- Lot
- Lots: 180952, exp Oct-19, 180953, exp Dec-19, 181086, exp Sep-19, 181572, exp Jan-20
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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