Warning
ACME UNITED CORPORATION Recalls Max Packaging Antibacterial Towelette (Benzalkonium.
This is a Class II recall. This product may cause temporary health problems or pose a slight threat of a serious nature.
Source: FDA
WarningRecall #D-0363-2026Drug / Pharmaceutical
ACME UNITED CORPORATION Recalls Max Packaging Antibacterial Towelette (Benzalkonium.
ACME UNITED CORPORATION · Class II — Moderate Risk
Product Description
Max Packaging Antibacterial Towelette (Benzalkonium Chloride 0.13%), 1 towelette, 4x7, Max Packaging, Made in the USA, NDC 59647-750-01
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