CLASS II Drug recall · Reported 27 Oct 2021 · FDA Enforcement Report
Cleaning Solutions Foaming Hand Sanitizer recalled by Sanitor
Sanitor is recalling Cleaning Solutions Foaming Hand Sanitizer, Active Ingredient Benzalkonium chloride 1%, distributed in Nevada. The recall was initiated on 21 Sep 2021 and the FDA has classified it as Class II.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0018-2022
- FDA event ID
- 88754
- Recalling firm
- Sanitor, Stanton, CA
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 21 Sep 2021
- FDA classified
- 15 Oct 2021
- Reported
- 27 Oct 2021
- Type
- Voluntary: Firm initiated
- Customers notified by
- Telephone
- Reason category
- Manufacturing (CGMP) Deviations
- Drug class
- Hand Sanitizer
Timeline
| 21 Sep 2021 | Recall initiated by company | |
| 15 Oct 2021 | Classified by FDA | +24 days |
| 27 Oct 2021 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
CGMP Deviations: Use of this product may cause possible infection/ irritation of the skin and/or soft tissues.
Product as listed by the FDA
Cleaning Solutions Foaming Hand Sanitizer, Active Ingredient Benzalkonium chloride 0.1%, New Wave Cleaning Solutions LLC, 7001 W Arby Ave Suite 100, Las Vegas, NV 89113, UPC#: 8 60001 93396 3
Where it was distributed
Distributed to one distributor located in Las Vegas, NV.
Questions about this recall
Is Cleaning Solutions Foaming Hand Sanitizer, Active Ingredient Benzalkonium chloride 1% recalled?
Yes. Sanitor recalled Cleaning Solutions Foaming Hand Sanitizer, Active Ingredient Benzalkonium chloride 1% on 21 Sep 2021. The recall is Class II and its status is Terminated. Recall number D-0018-2022.
Why was it recalled?
CGMP Deviations: Use of this product may cause possible infection/ irritation of the skin and/or soft tissues.
Which lots are affected?
Lot # 20102, 20103, Exp, Sept, 2021;
Where was it sold?
Distributed to one distributor located in Las Vegas, NV.
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.