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

Yes — there is an active recall. 12 ongoing FDA recalls mention Chloroxylenol (16 total). Check the affected lots below.

Most common reason: cGMP deviation (6 of these recalls)

Recalls are matched by product description. A recall usually affects specific lots, not every package of Chloroxylenol. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed. Checked against openFDA on Oct 10, 2026.

Chloroxylenol recalls on record

none so far in 2026; 16 on record, newest first
Class II · Moderate risk

PeriGiene

CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

Ongoing cGMP deviation DermaRite Industries, LLC NDC 61924-198-08 D-0172-2026
Class II · Moderate risk

KleenFoam Antimicrobial Foam Soap

CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

Ongoing cGMP deviation DermaRite Industries, LLC NDC 61924-093-34 D-0168-2026
Class II · Moderate risk

DermaKleen

CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

Ongoing cGMP deviation DermaRite Industries, LLC NDC 61924-092-08 D-0163-2026
Class I · High risk

PeriGiene

Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.

Ongoing Microbial contamination DermaRite Industries, LLC NDC 61924-198-08 D-0613-2025
Class I · High risk

KleenFoam

Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.

Ongoing Microbial contamination DermaRite Industries, LLC NDC 61924-093-34 D-0612-2025
Class I · High risk

DermaKleen

Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.

Ongoing Microbial contamination DermaRite Industries, LLC NDC 61924-092-27 D-0610-2025
Class II · Moderate risk

Medi-Stat 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 47593-503-59 D-0275-2019