RecallHawk
Class II Recall

Zep, Alcohol Sanitizer Spray, Ethanol 70%, Net Contents 55 Gallons 208 Liters, Made in USA, A Zep Inc. Brand, Distribute

Zep Inc

Summary

The FDA issued a Class II for Zep, Alcohol Sanitizer Spray, Ethanol 70%, Net Contents 55 Gallons 208 Liters, M by Zep Inc. Reason: Microbial contamination of sterile products.

Details

Source

Drug Recall

External ID

D-0586-2026

Action Date

2026-06-17

Status

Ongoing

Category

drug

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.

Lot/Code Info: Batch # E2612116, Exp Date: April 2029.

Quantity Affected: 5 drums

Reason for Recall

Microbial contamination of sterile products

Distribution

US Nationwide.

Type: Voluntary: Firm initiated

Recall Initiated: 2026-05-22

Company

Zep Inc

Emerson, GA

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 66 drug recalls issued in the same week, part of 267 drug-related FDA actions this month.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Zep Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Zep Inc have FDA actions?

This is the only FDA action we have on record for Zep Inc in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "D-0586-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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