Oxybutynin Chloride Tablets, USP, 5 mg, 500-count bottle, Rx only, Mfd. By: KVK-Tech, Inc., Newtown, PA 18940, NDC 10702-201-50
Reported: December 26, 2018 Initiated: December 11, 2018 #D-0340-2019
Product Description
Oxybutynin Chloride Tablets, USP, 5 mg, 500-count bottle, Rx only, Mfd. By: KVK-Tech, Inc., Newtown, PA 18940, NDC 10702-201-50
Reason for Recall
Labeling: Wrong bar code
Details
- Recalling Firm
- KVK-Tech, Inc.
- Units Affected
- 156 bottles
- Distribution
- Product was distributed by 10 major distributors throughout the United States.
- Location
- Newtown, PA
Frequently Asked Questions
What product 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. Recalled by KVK-Tech, Inc.. Units affected: 156 bottles.
Why was this product recalled? ▼
Labeling: Wrong bar code
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on December 26, 2018. Severity: Moderate. Recall number: D-0340-2019.
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