ACME UNITED CORPORATION Recalls Max Packaging Antibacterial Towelettes Due to CGMP Deviations
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
ACME UNITED CORPORATION has voluntarily recalled specific lots of Max Packaging Antibacterial Towelettes distributed nationwide due to manufacturing practice deviations.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on April 2, 2026 and geographically references United States. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, drugs.
What Happened
ACME UNITED CORPORATION, based in Shelton, CT, has initiated a voluntary recall of its Max Packaging Antibacterial Towelettes. The recall was triggered by deviations from Current Good Manufacturing Practice (CGMP) standards. The U.S. Food and Drug Administration (FDA) classified this as a Class II recall on March 2, 2026, indicating that the product may cause temporary or medically reversible adverse health consequences.
Which Products Are Affected
The recall involves Max Packaging Antibacterial Towelettes (Benzalkonium Chloride 0.13%), which are individual 4x7 towelettes. The products were distributed nationwide within the United States.
Product Details:
- Brand: Max Packaging
- NDC: 59647-750-01
- Recall Number: D-0363-2026
Affected Lot Numbers and Expiration Dates:
- Lot #: MN24523, Exp. Date: July 2028
- Lot #: MN27123, Exp. Date: Aug 2028
- Lot #: MN28223, Exp. Date: Sep 2028
What You Should Do
Consumers and distributors who have the affected lots of Max Packaging Antibacterial Towelettes should stop using the product immediately. ACME UNITED CORPORATION initiated the recall via notification letters. For further instructions regarding returns or disposal, parties may contact the firm at 1 Waterview Dr Ste 200, Shelton, CT 06484-4368.
Why This Matters
CGMP deviations indicate that the product was not manufactured under the strict quality control standards required by the FDA. This can lead to concerns regarding the product's safety, identity, strength, or purity.
Source
Information provided by the U.S. Food and Drug Administration (FDA).
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Frequently Asked Questions
Common questions about this FDA recall.