Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Oxybutynin Chloride Tablets Recalled by KVK-Tech, Inc. Due to Labeling: Wrong bar code
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact KVK-Tech, Inc. directly.
Affected Products
Oxybutynin Chloride Tablets, USP, 5 mg, 500-count bottle, Rx only, Mfd. By: KVK-Tech, Inc., Newtown, PA 18940, NDC 10702-201-50
Quantity: 156 bottles
Why Was This Recalled?
Labeling: Wrong bar code
Where Was This Sold?
Product was distributed by 10 major distributors throughout the United States.
About KVK-Tech, Inc.
KVK-Tech, Inc. has 13 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report