Acme United Corporation Recalls BZK Antiseptic Towelettes Due to Manufacturing Deviations
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Acme United Corporation has voluntarily recalled multiple brands of BZK Antiseptic Towelettes distributed nationwide due to Current Good Manufacturing Practice (CGMP) 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.
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What Happened
Acme United Corporation, based in Shelton, CT, has initiated a voluntary recall of several brands of BZK Antiseptic Towelettes (Benzalkonium Chloride 0.13%). The recall was prompted by Current Good Manufacturing Practice (CGMP) deviations. The FDA has classified this as a Class II recall, which was officially reported on March 11, 2026.
Which Products Are Affected
The recall affects 5"x7" towelettes sold in 1,000-count bulk quantities. The products were distributed nationwide within the United States. Affected brands and lot numbers include:
- Piedmont Sanitizing Hand Wipes (NDC 0924-7130-00): Lots MN22222, MN05523, MN32023, MN15523.
- Touchpoint BZK Antiseptic Towelettes (NDC 0924-7130-00): Lots MN11422B, MN11422, MN03823, MN09223, MN32123, MN20323, MN30822, MN304024, MN13023, MN12222, MN16023, MN27423.
- Wellstar Cobb Hand Wipes (NDC 0924-7130-00): Lots MN304024, MN13023, MN12222, MN16023, MN27423.
- FSR Sanitizing Hand Wipes (NDC 0924-7130-00): Lots MN04423, MN10022, MN30722, MN03523, MN09323, MN20223, MN32223.
- Children's Healthcare of Atlanta Hand Wipes (NDC 0924-713-00): Lots MN12122, MN27523, MN30922.
What You Should Do
Consumers and commercial users should immediately stop using the affected lots of antiseptic towelettes. Acme United Corporation initiated the recall via notification letters to its distributors and customers. For information regarding returns or additional questions, contact Acme United Corporation at 1 Waterview Dr Ste 200, Shelton, CT 06484.
Why This Matters
This recall is significant because the products were manufactured under conditions that deviated from established safety and quality standards (CGMP). A Class II recall indicates that the use of or exposure to the product may cause temporary or medically reversible adverse health consequences.
Source
Information provided by the FDA. Recall Number: D-0362-2026.
Original source: FDA Official Notice ↗
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