Teva North America recalls Capecitabine tablets USP 500 mg, Cytotoxic Agent, Rx Only, 120 tablets per bottle, Manufactured in Czech Republic by: Te
Recalled March 9, 2016 · FDA recall D-0732-2016 · Teva North America
Hazard
Failed Dissolution Specifications: low test results at the 18 month time-point · FDA Class II
Units
1,895 bottles
Sold at
Nationwide
Description
Failed Dissolution Specifications: low test results at the 18 month time-point
Product
Capecitabine tablets USP 500 mg, Cytotoxic Agent, Rx Only, 120 tablets per bottle, Manufactured in Czech Republic by: Teva Czech Industries sro, Czech Republic, Manufactured for: Teva Pharmaceuticals USA, Sellersville, PA 18960, NDC 0093-7474-89
Manufacturer(s)
Teva North America
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →