Class II · ModerateActive recall
Bzk Pads
Could cause temporary or reversible harm; serious harm is unlikely.
Does this affect you?
Check your lot numberLot #: 52347-R, 52348-R, 52349-R, 52350, 52351-R, 52352, Exp. Date Mar 2027; 53518, Exp. Date Jun 2027.
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
- Check the lot number and expiry on your medicine against the recall above.
- Talk to your pharmacist or doctor before changing anything — don't stop on your own.
- Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).
Who makes it
Made byDynarex Corporation
| Brand name | BZK PADS |
| Generic name | BENZALKONIUM CHLORIDE |
| Active ingredient(s) | BENZALKONIUM CHLORIDE |
| Distributed by / for | Dynarex Corporation, 10 Glenshaw Street, Orangeburg, NY 10962,USA |
| NDC | 67777-245-01 |
Show the full FDA record
| Full product label | Dynarex, BZK Antiseptic Towelettes (Benzalkonium Chloride 0.13%), 100 packets, 5x7, Manufactured for Dynarex Corporation, 10 Glenshaw Street, Orangeburg, NY 10962,USA, NDC 67777-245-01 |
| Recalling firm | ACME UNITED CORPORATION |
| Distribution | Nationwide within the United States |
| Quantity | N/A |
| Recall initiated | 2026-01-20 |
| Report date | 2026-03-11 |
| Recall completed | — |
| Recall number | D-0375-2026 |
| Classification | Class II |
| FDA status | Ongoing |
| Origin on file | Shelton CT United States |
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.