RECALL DATABASE

Soap Recall: KleenFoam Antimicrobial Foam with Aloe Vera

Announced 2025-11-26 · FDA

FDA is recalling KleenFoam Antimicrobial Foam Soap with Aloe Vera due to microbial contamination of a non-sterile drug product with Burkholderia cepacia. About 6,973 cartridges were distributed nationwide, with multiple lots and expiration dates listed. The recall includes several lots with expiration dates ranging from 8/2025 to 1/2027; no corrective action is listed.

BrandDermaRite Industries, LLC
ProductKleenFoam, Antimicrobial Foam Soap with Aloe Vera, (Chloroxylenol 0.5%) 34 FL OZ (1000 mL) per cartridge, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-093-34
ReasonMicrobial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.
Severitycritical
Units affected57837
DistributionNationwide within the USA
AgencyFDA

WHAT YOU SHOULD DO

  1. Do not use recalled KleenFoam Antimicrobial Foam Soap with Aloe Vera.
  2. Check your product's lot number against the recalled lots; if it matches, dispose of the cartridge or return it to the place of purchase for a refund or replacement.
  3. If you have questions, contact the retailer or DermaRite Industries for instructions.

How to identify the recalled item

Lot / date codesLot #: 30705A, Exp. Date 8/2025; 30771A, Exp. Date 9/2025; 30920A, Exp. Date 10/2025; 40016A, Exp. Date 1/2026; 40303A, Exp. Date 4/2026; 40428A, Exp. Date 5/2026; 40505A, Exp. Date 6/2026; 41053C, 41053A, 41053B, Exp. Date 12/2026, 50017A, Exp. Date 1/2027.
Lot / date codesAll lots on or before expiry date 08/2027

These are the identifiers FDA published for this recall. Most recall notices list no UPC or model number at all — if the code on your item is not shown here, that does not mean the item is excluded. Check the official notice, or contact the company.

This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.