FDAFDA recall D-0630-2026 · Jun 24, 2026
Dabur India Limited: Lucky Super Soft recall
Recall found
Product
Lucky Super Soft, First Aid Triple Antibiotic Ointment, Bacitracin zinc 400 units, neomycin sulphate 3.5 mg, polymyxin B sulphate 5000 units, Net Wt. 0.5 oz (14g) tubes, Manufactured for Delta Brands Inc., 580 White Plains Rd., Tarrytown, NY 10591 USA, Made in India, UPC 8 08829 10372 4.
Reason for recall
CGMP Deviations; deficiencies observed during FDA inspection
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your packaging. If this is a medicine or device you use, talk to your pharmacist or doctor before you stop or change anything, and contact the company or FDA for what to do with the product.
Recall details
- FDA classification
- Class II: use of or exposure to the product may cause temporary or medically reversible health problems, or the chance of serious problems is remote.
- Status
- Ongoing
- Codes, lots and dates
- Lot# 0002, Lot# 0003, within expiry
- Quantity
- 2503 tubes
- Distribution
- US Nationwide.
- Recalling firm
- Dabur India Limited, Dadra And Nagar Haveli
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2026-06-02
Source: openFDA enforcement record D-0630-2026 · search recall number D-0630-2026 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 22, 2026, 4:56 AM EDT. The agency notice is the final word.