Teva Pharmaceuticals USA, Inc recalls Budesonide Extended-Release Tablets 9mg, 30-count bottle, Rx Only, Manufactured by: Actavis Laboratories FL, Inc., Fort
Recalled February 7, 2024 · FDA recall D-0275-2024 · Teva Pharmaceuticals USA
Hazard
Failed Dissolution Specifications · FDA Class II
Units
10,672 30-count bottles
Sold at
Nationwide
Description
Failed Dissolution Specifications
Product
Budesonide Extended-Release Tablets 9mg, 30-count bottle, Rx Only, Manufactured by: Actavis Laboratories FL, Inc., Fort Lauderdale, FL 33314 USA, Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054 USA, NDC 0591-2510-30
Manufacturer(s)
Teva Pharmaceuticals USA, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →