Acuity Specialty Products, Inc.: Drug Recall

Recall #D-0004-2026 · 09/29/2025

Class II: Risk

Recall Details

Recall Number: D-0004-2026
Classification: Class II
Product Type: Drug
Recalling Firm: Acuity Specialty Products, Inc.
Status: Ongoing
Date Initiated: 09/29/2025
Location: Chambersburg, PA, United States
Voluntary/Mandated: Voluntary: Firm initiated

Reason for Recall

cGMP deviations: The recall was initiated because required receipt testing of incoming alcohol components used to manufacture the listed hand sanitizers was not performed, so methanol risk could not be excluded.

Product Description

Wyandotte, Sanifect E3, Hand Sanitizer (Ethanol-Based, Product 5511), Ethyl Alcohol 60.1%, Manufacture By: AFCO, 550 Development Avenue, Chambersburg, PA 17210, Toll Free: 800-345-1329, Package Configurations: a) 6x1000mL Case, b) 4x1 Gallon Case, c) 5 Gallon Pail, d) 55 Gallon Drum.

Distribution Pattern

US Nationwide.

Other Recalls by Acuity Specialty Products, Inc.

Class II: Risk 09/29/2025

cGMP deviations: The recall was initiated because required receipt testing of incoming alcohol components used to manufacture the listed hand sanitizers was not performed, so methanol risk could not be excluded.

View all recalls by Acuity Specialty Products, Inc. →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.