Severity
Moderate
ModerateClass IITerminated
FDA Drug recall · Reported October 27, 2021
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
CGMP Deviations: Use of this product may cause possible infection/ irritation of the skin and/or soft tissues.
Compiled from official public sources by the editorial team.
Verify with FDA Drug →
Sanitor Corporation recalled Cleaning Solutions Foaming Hand Sanitizer, Active Ingredient Benzalkonium chloride 0.1%, … - a moderate-severity action.
Cleaning Solutions Foaming Hand Sanitizer, Active Ingredient Benzalkonium chloride 0.1%, … was recalled by Sanitor Corporation in October 27, 2021. Reason: CGMP Deviations: Use of this product may cause possible infection/ irritation of the skin and/or soft tissues.. Check the official notice for the remedy. Verify recall #D-0018-2022 with the FDA Drug before acting.
The recall
Sanitor Corporation issued this moderate-severity FDA Drug recall-CGMP Deviations: Use of this product may cause possible infection/ irritation of the skin and/or soft tissues..
- Moderate
- severity level
- Class II
- classification
- October 27, 2021
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-0018-2022 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-0018-2022) was formally reported on October 27, 2021, with the manufacturer initiating the action on September 21, 2021. It is classified under Moderate severity (Class II), with a current status of Terminated. Sanitor Corporation is listed as the recalling firm, operating out of Stanton, CA. Federal records list the affected scope as unknown.
The documented reason for this recall is: CGMP Deviations: Use of this product may cause possible infection/ irritation of the skin and/or soft tissues. Distribution data in the federal record shows the product reached: Distributed to one distributor located in Las Vegas, NV.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 3 from FDA Drug - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Cosmetics & Personal Care recalls over time
Where this recall sits in its category - 1,360 cosmetics & personal care recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
unknown
Related Recalls
6
3 from same agency
Product description
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
Reason for recall
CGMP Deviations: Use of this product may cause possible infection/ irritation of the skin and/or soft tissues.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | D-0018-2022 |
| Date reported | October 27, 2021 |
| Date initiated | September 21, 2021 |
| Recalling firm | Sanitor Corporation |
| Firm location | Stanton, CA |
| Affected scope | unknown |
| Distribution | Distributed to one distributor located in Las Vegas, NV. |
Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (D-0018-2022) and product description against the item you own. Search the archive
- Confirm the current status with FDA Drug before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by Sanitor Corporation. Units affected: unknown.
Why was this product recalled? ▼
CGMP Deviations: Use of this product may cause possible infection/ irritation of the skin and/or soft tissues.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on October 27, 2021. Severity: Moderate. Recall number: D-0018-2022.
Where was the recalled product distributed? ▼
Distribution: Distributed to one distributor located in Las Vegas, NV..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-0018-2022) against your product. Visit the official FDA Drug website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
CPSC Moderate
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Drug, reported October 27, 2021. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.