Oxybutynin Chloride Tablets — Class II drug recall D-0340-2019
Terminated recall by KVK-Tech, Inc., reported 2018-12-26, distributed nationwide. Labeling: Wrong bar code
| Recall number | D-0340-2019 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | KVK-Tech, Inc., Newtown, PA, United States |
| Recall initiated | 2018-12-11 |
| Classified | 2018-12-19 |
| Reported by FDA | 2018-12-26 |
| Terminated | 2019-05-01 |
| Distributed | Nationwide (US) |
| Quantity | 156 bottles |
| Reason classes | labeling |
| NDC | 10702-0201, 10702-0201-01, 10702-0201-10, 10702-0201-50 |
| Lot numbers | 10/20, 15079A |
Product
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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0340-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.