Why it was recalled
CGMP Deviations
Product description
Max Packaging Antibacterial Towelette (Benzalkonium Chloride 0.13%), 1 towelette, 4x7, Max Packaging, Made in the USA, NDC 59647-750-01
Lot numbers, UPCs & expiration codes
Lot #: MN24523, Exp. Date July 2028; MN27123, Exp. Date Aug 2028; MN28223, Exp. Date Sep 2028.
Where it was sold
Nationwide within the United States
What to do if you have this product
- Compare the lot number and expiration date on your package with the codes above.
- Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
- If you have symptoms you think are related, contact your doctor. In an emergency call 911.
- Report side effects to FDA MedWatch at 1-800-FDA-1088.
Recall details
- Recall number
- D-0363-2026
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- Jan 20, 2026
- FDA report date
- Mar 11, 2026
- Quantity
- N/A
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- ACME UNITED CORPORATION
Original FDA data
Every field from FDA enforcement report D-0363-2026, exactly as published.
Show all FDA fields
- City
- Shelton
- State
- CT
- Status
- Ongoing
- Country
- United States
- Event ID
- 98291
- Address
- 1 Waterview Dr Ste 200
- Code information
- Lot #: MN24523, Exp. Date July 2028; MN27123, Exp. Date Aug 2028; MN28223, Exp. Date Sep 2028.
- Postal code
- 06484-4368
- Report date
- Mar 11, 2026
- Product type
- Drugs
- Recall number
- D-0363-2026
- Classification
- Class II
- Recalling firm
- ACME UNITED CORPORATION
- Reason for recall
- CGMP Deviations
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- Max Packaging Antibacterial Towelette (Benzalkonium Chloride 0.13%), 1 towelette, 4x7, Max Packaging, Made in the USA, NDC 59647-750-01
- Distribution pattern
- Nationwide within the United States
- Recall initiation date
- Jan 20, 2026
- Initial firm notification
- Letter
- Center classification date
- Mar 2, 2026