Dynarex BZK antiseptic towelettes recalled over manufacturing practice deviations
Acme United Corporation is recalling Dynarex BZK Antiseptic Towelettes in 100-packet cartons 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 Dynarex BZK Antiseptic Towelettes (Benzalkonium Chloride 0.13%), 100 packets, 5 x 7, made for Dynarex Corporation of Orangeburg, New York, NDC 67777-245-01. 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 52347-R, 52348-R, 52349-R, 52350, 52351-R and 52352 (expiry March 2027) and lot 53518 (expiry June 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
- BZK PADS (BENZALKONIUM CHLORIDE)
- Brand
- BZK PADS
- Manufacturer
- ACME UNITED CORPORATION
- Category
- Drug — Topical antiseptic
- Hazard
- gmp-deviation
- precautionary-recall
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 (9)
- Lot #: 52347-R
- 52348-R
- 52349-R
- 52350
- 52351-R
- 52352
- Exp. Date Mar 2027
- 53518
- Exp. Date Jun 2027.
UPCs (7)
- 0616784133225
- 0840117329331
- 0840117329355
- 0616784133324
- 0616784130323
- 0840117329379
- 0616784133133
Distribution
Distributed nationwide across the United States.
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