RecallHawk
Class II Recall

2% Chlorhexidine Gluconate* Cloth, Non-sterile, 6 Disposable cloths, Sage Products LLC, 3909 Three Oaks Road, Cary, Illi

Sage Products, LLC

Summary

The FDA issued a Class II for 2% Chlorhexidine Gluconate* Cloth, Non-sterile, 6 Disposable cloths, Sage Produc by Sage Products, LLC. Reason: Cross Contamination with Other Products.

Details

Source

Drug Recall

External ID

D-0837-2026

Action Date

2026-09-09

Status

Ongoing

Category

drug

Product Description

2% Chlorhexidine Gluconate* Cloth, Non-sterile, 6 Disposable cloths, Sage Products LLC, 3909 Three Oaks Road, Cary, Illinois 60013. NDC: 53462-705-26

Lot/Code Info: Lot 108491 with case sequence numbers 14841 through 20013.

Quantity Affected: 165,536 packages

Reason for Recall

Cross Contamination with Other Products

Distribution

US Nationwide.

Type: Voluntary: Firm initiated

Recall Initiated: 2026-08-18

Company

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 53 drug recalls issued in the same week, part of 66 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 (Sage Products, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Sage Products, LLC have FDA actions?

This is the only FDA action we have on record for Sage Products, LLC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "D-0837-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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