CLASS II ONGOING Drug recall · Reported 11 Mar 2026 · FDA Enforcement Report
WP WipesPlus Hand Sanitizing Wipes recalled by Acme United
Acme United is recalling WP WipesPlus Hand Sanitizing Wipes (Benzalkonium Chloride 13%), Progressive Products, 211, distributed nationwide in the US. The recall was initiated on 20 Jan 2026 and the FDA has classified it as Class II.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0372-2026
- FDA event ID
- 98291
- Recalling firm
- Acme United, Shelton, CT
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 20 Jan 2026
- FDA classified
- 2 Mar 2026
- Reported
- 11 Mar 2026
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Manufacturing (CGMP) Deviations
Timeline
| 20 Jan 2026 | Recall initiated by company | |
| 2 Mar 2026 | Classified by FDA | +41 days |
| 11 Mar 2026 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
CGMP Deviations
Product as listed by the FDA
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.
Where it was distributed
Nationwide within the United States
Questions about this recall
Is WP WipesPlus Hand Sanitizing Wipes (Benzalkonium Chloride 13%), Progressive Products, 211 recalled?
Yes. Acme United recalled WP WipesPlus Hand Sanitizing Wipes (Benzalkonium Chloride 13%), Progressive Products, 211 on 20 Jan 2026. The recall is Class II and its status is Ongoing. Recall number D-0372-2026.
Why was it recalled?
CGMP Deviations
Which lots are affected?
Lot #: MN27922, MN21722, MN21822, Exp. Date Jul 2027; MN27422, MN27522, Exp. Date Sep 2027; MN25422, Exp. Date Aug 2027; MN27922, MN27922, Exp. Date Sep 2027.
Where was it sold?
Nationwide within the United States
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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|---|---|---|---|---|---|
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