Dynarex 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 Dynarex, BZK Antiseptic Towelettes (Benzalkonium Chloride 0.13%), 5x7, 1000 packets, 5x7, Manufactured for Dynarex Corp…
- Recall number
- D-0376-2026
- 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
Dynarex, BZK Antiseptic Towelettes (Benzalkonium Chloride 0.13%), 5x7, 1000 packets, 5x7, Manufactured for Dynarex Corporation, 10 Glenshaw Street, Orangeburg, NY 10962,USA, NDC 67777-245-04.
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