US Drug Recall Register
Class II · Moderate risk Terminated Initiated Dec 11, 2018 (8 years ago)

Oxybutynin Chloride Tablets, USP, 5 mg, 500-count bottle, Rx only, Mfd. By: KVK-Tech…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Labeling: Wrong bar code

What was recalled

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

Recalling firm
KVK-Tech, Inc.
NDC code
10702-201-50
Origin
PA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0340-2019

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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