Dukal BZK Antiseptic Towelette 1000 Packs per case recalled over manufacturing violations
- Recall date
- January 20, 2026
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- ACME UNITED CORPORATION recalls Dukal BZK Antiseptic Towelette (Benzalkonium Chloride 0.13%) 1000 Packs per case, Manufactured For: Dukal, LLC, Ronkonk…
- Recall number
- D-0360-2026
- FDA classification
- Class II
- Brand / firm
- ACME UNITED CORPORATION
- Sold / distributed
- Nationwide within the United States
Why it was recalled
CGMP Deviations
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Dukal BZK Antiseptic Towelette (Benzalkonium Chloride 0.13%) 1000 Packs per case, Manufactured For: Dukal, LLC, Ronkonkoma, NY 11779, Made in USA, NDC 65517-0004-1
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