Bzk Pads Swab
FDA Recall NDC 67777-245
FDA Enforcement Report: View Recall Date, Reasons, and Safety Status
Active & Historical Enforcement Reports
The FDA has identified 2 recorded enforcement report(s) associated with Bzk Pads (NDC 67777-245). A significant event, classified as Class II, was initiated on Jan 20, 2026 by Dynarex Corporation. The reported reason for this action was: "CGMP Deviations"
This recall is currently ONGOING. Healthcare providers and patients are advised to check their inventory immediately against the affected codes provided below.
This recall is currently ONGOING. Healthcare providers and patients are advised to check their inventory immediately against the affected codes provided below.
Reported Recall Events
Class II Ongoing
CGMP Deviations
Jan 20, 2026
Mar 11, 2026
N/A
Recall Profile & Regulatory Data
Event ID
98291
Classification
Class II
Enforcement Status
Ongoing
Recalling Firm
ACME UNITED CORPORATION
Voluntary / Mandated
Voluntary: Firm initiated
Distribution Pattern
Nationwide within the United States
Product Description
Dynarex, BZK Antiseptic Towelettes (Benzalkonium Chloride 0.13%), 5x7, 1000 packets, 5x7, Manufactured for Dynarex Corporation, 10 Glenshaw Street, Orangeburg, NY 10962,USA, NDC 67777-245-04.
Batch or Lot Expiration Information
Lot# : 53518, 53519, Exp. Date Jun 2027.
Affected Packages Involved in this Recall
67777-245-01Product
67777-245-11Product
67777-245-02Product
67777-245-14Product
67777-245-04Product
67777-245-15Product
67777-245-05Product
67777-245-06Product
67777-245-16Product
67777-245-08Product
67777-245-18Product
67777-245-07Product
67777-245-17Product
Class II Ongoing
CGMP Deviations
Jan 20, 2026
Mar 11, 2026
N/A
Recall Profile & Regulatory Data
Event ID
98291
Classification
Class II
Enforcement Status
Ongoing
Recalling Firm
ACME UNITED CORPORATION
Voluntary / Mandated
Voluntary: Firm initiated
Distribution Pattern
Nationwide within the United States
Product Description
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
Batch or Lot Expiration Information
Lot# : 52347-R, 52348-R, 52349-R, 52350, 52351-R, 52352, Exp. Date Mar 2027; 53518, Exp. Date Jun 2027.
Affected Packages Involved in this Recall
67777-245-01Product
67777-245-11Product
67777-245-02Product
67777-245-14Product
67777-245-04Product
67777-245-15Product
67777-245-05Product
67777-245-06Product
67777-245-16Product
67777-245-08Product
67777-245-18Product
67777-245-07Product
67777-245-17Product
About FDA Recall Enforcement Reports
FDA recall data documents classified recall actions associated with a product. Most recalls are limited to specific lots, batches, or package configurations rather than every unit of a drug.
If a recall is listed for an NDC, review the affected lot information and package details carefully. Patients and healthcare professionals should confirm whether a specific product in hand matches the lot or package information before assuming it is affected.
