Oxybutynin Chloride Tablets, USP, 5 mg, 500-count bottle, Rx only, Mfd. By: KVK-Tech, Inc., Newtown, PA 18940, NDC 10702-201-50

FDA recall notice · announced December 26, 2018 · Kvk-tech

Class II FDA/FSIS Class II: use may cause temporary or medically reversible adverse health consequences.

The product

Reason for recall

Labeling: Wrong bar code

Notes

Distribution: Product was distributed by 10 major distributors throughout the United States.
Lot/code information: Lot #: 15079A, Exp 10/20
Quantity: 156 bottles
Status: Terminated
Products in this recall event:
- Oxybutynin Chloride Tablets, USP, 5 mg, 500-count bottle, Rx only, Mfd. By: KVK-Tech, Inc., Newtown, PA 18940, NDC 10702-201-50 (D-0340-2019)

Source: U.S. Food and Drug Administration public recall data. This page reports official records and is not legal, medical, or repair advice.