Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Class II · Moderate risk Terminated Initiated Mar 29, 2021 (6 years ago)

Lite'n Foamy Healthcare Personnel Handwash (Chloroxylenol)

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

CGMP Deviations

Cause type: cGMP deviation

Departures from current Good Manufacturing Practice found in production or during FDA inspection. A broad quality-system cause: the batch was made under conditions that fall short of FDA manufacturing standards. All cgmp deviation recalls.

What was recalled

Lite'n Foamy Healthcare Personnel Handwash (Chloroxylenol, 1.0%), Net Contents: 18 oz/ 532 ml per foam pump container, For Institutional and Industrial Use Only, Spartan Chemical Company, Inc., 1110 Spartan Drive, Maumee, OH 43537 USA. UPC 7 53727 26283 0 NDC: 64009-335-82

Affected NDC 64009-0335-82

Compare with the code on your package — it is the most precise check available.

Drug: Chloroxylenol

Product details

From the FDA NDC directory, for the product code this recall names. Compare with the label on your package.

ProductStrengthForm & routeLabelerType
Lite nFoamy Healthcare Personnel Handwash
Chloroxylenol
NDC 64009-0335
10.11 g/L Soap
Topical
Spartan Chemical Company OTC
Recalling firm
Spartan Chemical Co Inc
Origin
OH, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0364-2021 · FDA notice

Check, then ask. Class II means harm is possible but usually temporary or reversible. Find the lot number on your package; if it matches, ask your pharmacist about a replacement. Do not simply stop a prescribed medication on your own - the gap can be riskier than the recall. This recall is now terminated, which means the firm has finished removing the affected product; anything on pharmacy shelves today should be unaffected.

Other Chloroxylenol recalls

See all
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

Other recalls by Spartan Chemical Co Inc

All 2021 recalls