Acuity Specialty Products, Inc.

FDA Regulatory Profile

Acuity Specialty Products, Inc. appears in FDA public data with 2 recalls, 0 510(k) clearances, 5 FDA inspections, and 1 compliance action on record. Its most recent recall (D-0005-2026, Class II) was initiated on September 29, 2025.

Summary

Total Recalls
2
510(k) Clearances
0
Inspections
5
Compliance Actions
1

Recent Recalls

NumberClassProductDate
D-0005-2026Class IIAFCO, Hand Sanitizer (Isopropyl Alcohol-Based, Product 5515), Manufactured by: AFCO, 550 DevelopmentSeptember 29, 2025
D-0004-2026Class IIWyandotte, Sanifect E3, Hand Sanitizer (Ethanol-Based, Product 5511), Ethyl Alcohol 60.1%, ManufactuSeptember 29, 2025