Rapidol — Class II drug recall D-0633-2026
Ongoing recall by Dabur India Limited, reported 2026-06-24, distributed nationwide. CGMP Deviations; deficiencies observed during FDA inspection
| Recall number | D-0633-2026 |
|---|---|
| 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 | 84 tubes |
| Reason classes | cgmp |
| UPC / GTIN / UDI-DI | 00810096771629 |
| Lot numbers | 0004 |
Product
Rapidol, Triple Antibiotic First Aid Ointment, Bacitracin Zinc 400 units, Neomycin Sulfate 3.5 mg, Polymyxin-B Sulfate 5,000 units, net wt. 2oz (57g) tubes, Distributed by/por: Pharmadel LLC, New Castle, DE 19720, Made in India, UPC 8 10096 77162 9.
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-0633-2026. 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.