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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 notice