PROBLEND E3 Foaming Hand Sanitizer recalled over manufacturing violations

Recall date

February 19, 2024

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Official notice title

Seatex LLC recalls PROBLEND E3 Foaming Hand Sanitizer, All-In-One Foaming Hand Sanitizer & Cleanser, Seatex LLC, 445 TX Hwy 36 Rosenberg,…

Recall number

D-0357-2024

FDA classification

Class II

Brand / firm

Seatex LLC

Sold / distributed

Nationwide in the US and Puerto Rico

Why it was recalled

CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

PROBLEND E3 Foaming Hand Sanitizer, All-In-One Foaming Hand Sanitizer & Cleanser, Seatex LLC, 445 TX Hwy 36 Rosenberg, TX 77471