KVK-Tech, Inc. recalls Oxybutynin Chloride Tablets, USP, 5 mg, 500-count bottle, Rx only, Mfd. By: KVK-Tech, Inc., Newtown, PA 18940, NDC 1070…
- Recall date
- December 11, 2018
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-0340-2019
- FDA classification
- Class II
- Brand / firm
- KVK-Tech, Inc.
- Sold / distributed
- Product was distributed by 10 major distributors throughout the United States.
Why it was recalled
Labeling: Wrong bar code
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
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
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