RecallRadar

FDA Drug recall D-0356-2024

PROBLEND Antibacterial Foaming Silk All-In-One Foaming Hand Sanitizer & Cleanser, Benzalkonium Chloride 0.13% Antibacterial, a) 1250 mL cas…

On 2024-03-06 the FDA classified a Class II recall of PROBLEND Antibacterial Foaming Silk All-In-One Foaming Hand Sanitizer & Cleanser, Benzalkonium Chloride 0.13% Antibacterial, a) 1250 mL cas… by Seatex, citing CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0356-2024
ClassificationClass II
Statusterminated
Initiated2024-02-19
Published2024-03-06
Last updated2026-09-13 11:52 UTC
CompanySeatex
DistributionUS

Product

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.

Reason

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

Identifiers

code_infoLot #s: a) 263647, Exp. 06/09/2024; 271382, Exp. 01/18/2025; b) 261675, Exp. 04/09/2024; 263647, Exp. 06/09/2024; 272766, Exp.02/15/2025.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0356-2024%22

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