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Class II · ModerateActive recall

Bzk Towelette

Could cause temporary or reversible harm; serious harm is unlikely.

Does this affect you?
Check your lot numberLot #: MN31621, Exp. Date Oct 2026; MN14522, MN15522, Exp. Date Apr 2027; MN28122, MN31522, Exp. Date Sept 2027; MN04223, MN06023, Exp. Date Feb 2028; MN17223, Exp. Date May 2028; MN25123, Exp Date Aug 2028; MN33123, MN33523, Exp. Date Nov 2028.
Where it was soldNationwide within the United States
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

CGMP Deviations

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byMade in USA
Brand nameBZK TOWELETTE
Generic nameBENZALKONIUM CHLORIDE
Active ingredient(s)BENZALKONIUM CHLORIDE
Distributed by / forDukal, LLC, Ronkonkoma, NY 11779, Made in USA
NDC65517-0004-1
Show the full FDA record
Full product labelDukal BZK Antiseptic Towelette (Benzalkonium Chloride 0.13%) 1000 Packs per case, Manufactured For: Dukal, LLC, Ronkonkoma, NY 11779, Made in USA, NDC 65517-0004-1
Recalling firmACME UNITED CORPORATION
DistributionNationwide within the United States
QuantityN/A
Recall initiated2026-01-20
Report date2026-03-11
Recall completed—
Recall numberD-0360-2026
ClassificationClass II
FDA statusOngoing
Origin on fileShelton CT United States

Related

Recent drug recallsCheck another medication

Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.