KVK-Tech, Inc. recalls Oxybutynin Chloride Tablets, USP, 5 mg, 500-count bottle, Rx only, Mfd. By: KVK-Tech, Inc., Newtown, PA 18940, NDC 10702
Recalled December 26, 2018 · FDA recall D-0340-2019 · KVK-Tech
Hazard
Labeling: Wrong bar code · FDA Class II
Units
156 bottles
Sold at
Product was distributed by 10 major distributors throughout the United States.
Description
Labeling: Wrong bar code
Product
Oxybutynin Chloride Tablets, USP, 5 mg, 500-count bottle, Rx only, Mfd. By: KVK-Tech, Inc., Newtown, PA 18940, NDC 10702-201-50
Manufacturer(s)
KVK-Tech, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →