ACME UNITED CORPORATION Recalls Dukal BZK Antiseptic Towelette (Benzalkonium Chloride 0
This is a Class II recall. This product may cause temporary health problems or pose a slight threat of a serious nature.
ACME UNITED CORPORATION Recalls Dukal BZK Antiseptic Towelette (Benzalkonium Chloride 0
ACME UNITED CORPORATION · Class II — Moderate Risk

Product Description
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
Reason for Recall
CGMP Deviations
FDA Classification
Class II — Moderate Risk
A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
Distribution
Nationwide within the United States
Remedy
Consumers should stop using this product. Contact the recalling firm for further instructions regarding this product.
Sources: FDA openFDA Enforcement Database