Reported Oct 15, 2025 · Ongoing
Wyandotte, Sanifect E3, Hand Sanitizer (Ethanol-Based, Product 5511), Ethyl Alcohol 60.1%, Manufacture By
Acuity Specialty Products, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Acuity Specialty Products, Inc. · 800 Development Ave · Chambersburg, PA · 17201-4103
Is this the product you have?
Wyandotte, Sanifect E3, Hand Sanitizer (Ethanol-Based, Product 5511), Ethyl Alcohol 60.1%, Manufacture By
4 of 4 products
| # | Product as published |
|---|---|
| 1 | 6x1000mL Case |
| 2 | 4x1 Gallon Case |
| 3 | 5 Gallon Pail |
| 4 | 55 Gallon Drum. |
- Lot codes and dates
Lot # C2427010Exp 9/26/2025Lot # C2432621Exp 11/21/2025Lot # C2501514Exp 1/15/2026Lot # C2508606Exp 3/27/2026
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
- Nationwide
Why it was recalled
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.
This product could cause temporary or reversible health problems — stop using it.
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