US Drug Recall Register
Class II · Moderate risk Terminated Initiated Feb 19, 2024 (3 years ago)

PROBLEND Antibacterial Foaming Silk All-In-One Foaming Hand Sanitizer & Cleanser…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

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

What was recalled

PROBLEND Antibacterial Foaming Silk All-In-One Foaming Hand Sanitizer & Cleanser, Benzalkonium Chloride 0.13% Antibacterial, a) 1250 mL cases, b) 1 G cases, mountain spring scent, Seatex LLC, 445 TX Hwy 36 Rosenberg, TX 77471.

Recalling firm
Seatex LLC
Origin
TX, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0356-2024

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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