FDA · Drugs ·
Circle K, triple antibiotic ointment recall
Dabur India Limited recalled Circle K, triple antibiotic ointment on June 24, 2026 because of cGMP Deviations; deficiencies observed during FDA inspection. It was sold nationwide.
Why it was recalled
CGMP Deviations; deficiencies observed during FDA inspection
What's recalled
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.
Quantity: 2420 tubes
What to do
Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.
Read the official FDA noticeDetails
- Company
- Dabur India Limited, Dadra And Nagar Haveli
- Date
- Severity
- Class II
the product could cause temporary or reversible health problems. - Where sold
- Nationwide
US Nationwide. - Status
- Ongoing
- Recall number
- D-0631-2026
- Source
- U.S. Food and Drug Administration
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