Circle K — Class II drug recall D-0631-2026
Ongoing recall by Dabur India Limited, reported 2026-06-24, distributed nationwide. CGMP Deviations; deficiencies observed during FDA inspection
| Recall number | D-0631-2026 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Dabur India Limited, Dadra And Nagar Haveli, India |
| Recall initiated | 2026-06-02 |
| Classified | 2026-06-26 |
| Reported by FDA | 2026-06-24 |
| Distributed | Nationwide (US) |
| Quantity | 2,420 tubes |
| Reason classes | cgmp |
| UPC / GTIN / UDI-DI | 00194283651810 |
| Lot numbers | 0001, 0005 |
Product
Circle K, triple antibiotic ointment, Bacitracin Zinc (400 units), Neomycin Sulfate (3.5 mg), Polymyxin-B Sulfate (5000 units), net wt. 0.5 oz (14.2g) tubes, Product manufactured for Lil' Drug Store Products, Inc., 9300 Earhart Lane SW, Cedar Rapids, IA 52404, Made in India, UPC 1 94283 65181 0.
Reason for recall
CGMP Deviations; deficiencies observed during FDA inspection
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-0631-2026. 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.