Med Nap Cleansing Towelette Liquid
FDA Recall NDC 0924-0243
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 Med Nap Cleansing Towelette (NDC 0924-0243). 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
Cleansing Towelette (Benzalkonium Chloride 0.13%), 5"x 7", 1,000 case/Bulk, Med-Nap, Brooksville, FL 34601, Made in USA, NDC 0924-0243-00.
Batch or Lot Expiration Information
Lot# : MN15923, Exp. Date May 2028; MN25822, Exp. Date Aug 2027.
Affected Packages Involved in this Recall
0924-0243-00Product
0924-0243-01Product
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
Med-Nap Cleansing Towelettes (Benzalkonium Chloride 0.13%), 100 Towelettes, Manufactured by: Acme United Corporation, 1 Waterview Dr., Stelton, CT 06484, NDC 0924-0243-01.
Batch or Lot Expiration Information
Lot# : 52347, 52348, 52349, 52350, 52351, Exp. Date Mar 2027.
Affected Packages Involved in this Recall
0924-0243-00Product
0924-0243-01Product
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.
