The Recall Desk
ModerateFDA (Drugs)·D-0372-2026·Announced 2026-03-11

WipesPlus hand sanitizing wipes recalled over manufacturing practice deviations

Acme United Corporation is recalling WP WipesPlus Hand Sanitizing Wipes over current good manufacturing practice deviations.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: Rubric level 2 covers voluntary precautionary recalls: this is a firm-initiated recall over manufacturing practice deviations with no hazard, illness or injury described in the source.

Plain-English summary

Acme United Corporation is recalling WP WipesPlus Hand Sanitizing Wipes (Benzalkonium Chloride 0.13%), 5 x 7, 100 count, for Progressive Products of Rye Brook, New York, NDC 67151-727-01. The product was distributed nationwide within the United States. The FDA has classified this recall as Class II, and the firm initiated it voluntarily.

The recall was initiated for CGMP deviations. The source record does not describe a specific hazard, illness or injury.

Affected product covers lots MN27922, MN21722, MN21822, MN27422, MN27522 and MN25422, with expiry dates from July 2027 to September 2027.

Users can identify affected product by the NDC and lot numbers above, and may contact Acme United Corporation for further information.

The recalled product

Product
WP WipesPlus Hand Sanitizing Wipes (Benzalkonium Chloride 0.13%), 5x7, 100 CT, Progressive Products, 211 S. Ridge Street, Rye Brook, NY 10573. NDC 67151-727-01.
Manufacturer
ACME UNITED CORPORATION
Category
Drug — Topical antiseptic
Hazard

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (11)

  • Lot #: MN27922
  • MN21722
  • MN21822
  • Exp. Date Jul 2027
  • MN27422
  • MN27522
  • Exp. Date Sep 2027
  • MN25422
  • Exp. Date Aug 2027
  • MN27922
  • Exp. Date Sep 2027.

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 21 recalled by ACME UNITED CORPORATION under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 21 products in this recall →

Related recalls

Same manufacturer · ACME UNITED CORPORATION

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Same hazard · gmp deviation

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