Fresh Recalls

Circle K: recall status

Notice names this product. Dabur India’s Circle K is named in FDA Class II recall D-0631-2026. Your particular item is not yet verified. Compare the identifiers and exclusions in the notice before deciding whether it applies. Agency-reported hazard: CGMP Deviations; deficiencies observed during FDA inspection Identifying details: Lot# 0001, and Lot# 0005, within expiry. Units affected: 2420 tubes. Status: Ongoing.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Circle K
Company / brand
Dabur India
Lot / serial / date codes
Lot# 0001, and Lot# 0005, within expiry
Distribution
US Nationwide.
Agency product description and boundaries

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.

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

Brand
Dabur India

Recalls naming this model

FDA Class II · Drug · June 24, 2026

Circle K recall — Dabur India Limited

CGMP Deviations; deficiencies observed during FDA inspection

Company / brand: Dabur India

Affected product: Circle K

Official ID D-0631-2026 · Official record ↗

See all Dabur India recalls →

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Compiled from connected official public-domain government data. Sources last checked September 7, 2026 at 6:00 AM UTC.