PROBLEND Antibacterial Foaming Silk All-In-One Foaming Hand Sanitizer & Cleanser
CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
Yes — there is an active recall. 25 ongoing FDA recalls mention Benzalkonium (77 total). Check the affected lots below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Benzalkonium. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed. Checked against openFDA on Oct 10, 2026.
CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
CGMP Deviations
Microbial Contamination of Non-Sterile Products: FDA Laboratory results found product to be contaminated with Bacillus lichenformis and Bacillus sonorensis.
Chemical Contamination and CGMP Deviations: trace amounts of methanol found in one of the components during the manufacturing process.
Chemical Contamination and CGMP Deviations: trace amounts of methanol found in one of the components during the manufacturing process.
CGMP Deviations: Product manufactured using expired active ingredient, Benzalkonium chloride.
CGMP Deviations: Product manufactured using expired active ingredient, Benzalkonium chloride.
Microbial Contamination of Non-sterile Product; FDA analysis found the product to be contaminated with Bacillus cereus.
CGMP Deviations: Use of this product may cause possible infection/ irritation of the skin and/or soft tissues.
Lack of Assurance of Sterility: FDA inspection raised sterility assurance concerns
CGMP Deviations
CGMP Deviations
CGMP Deviations
Microbial Contamination of Non-Sterile Products; lot tested positive for Bulkholderia multivorans
CGMP Deviations: lots recalled due to CGMP deviations because they were manufactured under the same conditions as product lots found to be contaminated.
CGMP Deviations: lots recalled due to CGMP deviations because they were manufactured under the same conditions as product lots found to be contaminated.
Microbial Contamination of Non-Sterile Products: firm's internal testing found certain lots of the product to be contaminated with Burkholderia contaminans and/or yeast and mold.
Microbial Contamination of Non-Sterile Products: firm's internal testing found certain lots of the product to be contaminated with Burkholderia contaminans and/or yeast and mold.
Microbial contamination of non-sterile products: positive microbial contamination in product.
Lack of Assurance of Sterility
CGMP Deviations: hand sanitizers and soaps were not produced under current good manufacturing practices.
Microbial Contamination of Non-Sterile Product: Presence of Pseudomonas aeruginosa in product
Labeling: Label mix-up - the label on the product may not match the formula in the bottle.
CGMP Deviations: Product was released to market prior to microbiological testing.
CGMP Deviations: Product was released to market prior to microbiological testing.
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