Dabur India Limited — Circle K recall — Check your batch

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Dabur India Limited

Check your batch

Check the batch codes below. If yours matches, return it for a refund rather than take it.

Class II

May cause temporary or medically reversible harm. Serious consequences are unlikely.
Refunds don't require a receipt, and you don't need proof of purchase.
FDA status: Ongoing.

What was recalled

Source: FDA · synced 29 Jul 2026 13:14

Check your batch Filed 2026-06-24

CGMP Deviations; deficiencies observed during FDA inspection

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.

Check these codes: Lot# 0001, and Lot# 0005, within expiry

2420 tubes · distributed us nationwide. Recall D-0631-2026 on FDA.gov ↗

Watch Dabur India Limited for new recalls

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