Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Is Benzalkonium recalled?

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.

Benzalkonium recalls on record

none so far in 2026; 77 on record, newest first
Class I · High risk

Easy Care first aid Burn Cream

Microbial Contamination of Non-Sterile Products: FDA Laboratory results found product to be contaminated with Bacillus lichenformis and Bacillus sonorensis.

Terminated Microbial contamination GFA Production Xiamen Co. Ltd. D-0244-2023
Class II · Moderate risk

Proton Armor

Chemical Contamination and CGMP Deviations: trace amounts of methanol found in one of the components during the manufacturing process.

Terminated Chemical / undeclared Ultra Chem Labs Corp NDC 79208-001-50 D-0017-2023
Class II · Moderate risk

Proton Armor

Chemical Contamination and CGMP Deviations: trace amounts of methanol found in one of the components during the manufacturing process.

Terminated Chemical / undeclared Ultra Chem Labs Corp NDC 79208-001-50 D-0016-2023
Class I · High risk

Revitaderm Wound Care Gel

Microbial Contamination of Non-sterile Product; FDA analysis found the product to be contaminated with Bacillus cereus.

Terminated Microbial contamination Blaine Labs Inc NDC 63347-120-02 D-0668-2022
Class II · Moderate risk

Durisan Antimicrobial Solutions

CGMP Deviations: lots recalled due to CGMP deviations because they were manufactured under the same conditions as product lots found to be contaminated.

Terminated cGMP deviation Sanit Technologies, LLC dba Durisan D-0659-2021
Class II · Moderate risk

Durisan Antimicrobial Solutions

CGMP Deviations: lots recalled due to CGMP deviations because they were manufactured under the same conditions as product lots found to be contaminated.

Terminated cGMP deviation Sanit Technologies, LLC dba Durisan D-0658-2021
Class I · High risk

Durisan Antimicrobial Solutions

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.

Terminated Microbial contamination Sanit Technologies, LLC dba Durisan D-0657-2021
Class I · High risk

Durisan Antimicrobial Solutions

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.

Terminated Microbial contamination Sanit Technologies, LLC dba Durisan D-0656-2021
Class II · Moderate risk

Equi-Soft Foam

Labeling: Label mix-up - the label on the product may not match the formula in the bottle.

Terminated Labeling / mix-up Ecolab Inc NDC 47593-521-41 D-0274-2019
Class II · Moderate risk

deb stoko

CGMP Deviations: Product was released to market prior to microbiological testing.

Terminated Microbial contamination S.C. Johnson Professional NDC 11084-010-27 D-0220-2019