First Aid Only Hand Sanitizing Wipe Swab
FDA Recall NDC 0924-0301
FDA Enforcement Report: View Recall Date, Reasons, and Safety Status
Active & Historical Enforcement Reports
The FDA has identified 1 recorded enforcement report(s) associated with First Aid Only Hand Sanitizing Wipe (NDC 0924-0301). A significant event, classified as Class II, was initiated on Jan 20, 2026 by Acme United 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
Hand Sanitizing Wipes (Benzalkonium Chloride 0.13%), 1000 per case, Acme United Corporation, 2280 Tanner Road, Rocky Mount, NC 27801, NDC 0924-0301-00
Batch or Lot Expiration Information
Lot# : MN24922, Exp. Date Aug 2027; MN31122, Exp. Date Oct 2027.
Affected Packages Involved in this Recall
0924-0301-00Product
0924-0301-04Product
0924-0301-05Product
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.
