PROBLEND E3 Foaming Hand Sanitizer, All-In-One Foaming Hand Sanitizer & Cleanser, Seatex LLC, 445...

FDA Recall #D-0357-2024 — Class II — February 19, 2024

Recall #D-0357-2024 Date: February 19, 2024 Classification: Class II Status: Terminated

Product Description

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

Reason for Recall

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

Recalling Firm

Seatex LLC — Rosenberg, TX

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Drugs

Product Quantity

274 cases

Distribution

Nationwide in the US and Puerto Rico

Code Information

Lot #: 265029, Exp. 03/27/2024; 273759, Exp. 11/29/2024.

Status

Terminated

Voluntary / Mandated

Voluntary: Firm initiated