Zep Alcohol Sanitizer Liquid
FDA Recall NDC 66949-133
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 Zep Alcohol Sanitizer (NDC 66949-133). A significant event, classified as Class II, was initiated on May 22, 2026 by Zep Inc.. The reported reason for this action was: "Microbial contamination of sterile products"
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
Microbial contamination of sterile products
May 22, 2026
Jun 17, 2026
5 drums
Recall Profile & Regulatory Data
Event ID
99112
Classification
Class II
Enforcement Status
Ongoing
Recalling Firm
Zep Inc
Voluntary / Mandated
Voluntary: Firm initiated
Distribution Pattern
US Nationwide.
Product Description
Zep, Alcohol Sanitizer Spray, Ethanol 70%, Net Contents 55 Gallons 208 Liters, Made in USA, A Zep Inc. Brand, Distributed by: Zap Inc., 350 Joe Frank Harris Parkway, SE, Emerson, GA 30137, NDC 66949-133-85.
Batch or Lot Expiration Information
Batch# E2612116, Exp Date: April 2029.
Affected Packages Involved in this Recall
66949-133-24Product
66949-133-85Product
66949-133-01Product
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.
