FDA Drug Recalls

Recalls / Class II

Class IID-0375-2026

Product

Dynarex, BZK Antiseptic Towelettes (Benzalkonium Chloride 0.13%), 100 packets, 5x7, Manufactured for Dynarex Corporation, 10 Glenshaw Street, Orangeburg, NY 10962,USA, NDC 67777-245-01

Brand name
Bzk Pads
Generic name
Benzalkonium Chloride
Active ingredient
Benzalkonium Chloride
Route
Topical
NDC
67777-245
FDA application
M003
Affected lot / code info
Lot #: 52347-R, 52348-R, 52349-R, 52350, 52351-R, 52352, Exp. Date Mar 2027; 53518, Exp. Date Jun 2027.

Why it was recalled

CGMP Deviations

Recalling firm

Firm
ACME UNITED CORPORATION
Manufacturer
Dynarex Corporation
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
1 Waterview Dr Ste 200, N/A, Shelton, Connecticut 06484-4368

Distribution

Quantity
N/A
Distribution pattern
Nationwide within the United States

Timeline

Recall initiated
2026-01-20
FDA classified
2026-03-02
Posted by FDA
2026-03-11
Status
Ongoing

Source: openFDA Drug Enforcement endpoint. Recall record D-0375-2026. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.