Why it was recalled
CGMP Deviations; deficiencies observed during FDA inspection
Product description
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.
Lot numbers, UPCs & expiration codes
Lot# 0001, and Lot# 0005, within expiry
Where it was sold
US Nationwide.
What to do if you have this product
- Compare the lot number and expiration date on your package with the codes above.
- Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
- If you have symptoms you think are related, contact your doctor. In an emergency call 911.
- Report side effects to FDA MedWatch at 1-800-FDA-1088.
Recall details
- Recall number
- D-0631-2026
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- Jun 2, 2026
- FDA report date
- Jun 24, 2026
- Quantity
- 2420 tubes
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Dabur India Limited
Original FDA data
Every field from FDA enforcement report D-0631-2026, exactly as published.
Show all FDA fields
- City
- Dadra And Nagar Haveli
- Status
- Ongoing
- Country
- India
- Event ID
- 99137
- Address
- 225 - 4 - 1 Saily Village
- Address (line 2)
- Survey No
- Code information
- Lot# 0001, and Lot# 0005, within expiry
- Report date
- Jun 24, 2026
- Product type
- Drugs
- Recall number
- D-0631-2026
- Classification
- Class II
- Recalling firm
- Dabur India Limited
- Product quantity
- 2420 tubes
- Reason for recall
- CGMP Deviations; deficiencies observed during FDA inspection
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- 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.
- Distribution pattern
- US Nationwide.
- Recall initiation date
- Jun 2, 2026
- Initial firm notification
- Center classification date
- Jun 26, 2026