Sanitor Corporation: Drug Recall
Recall #D-0018-2022 · 09/21/2021
Class II: Risk
Recall Details
- Recall Number
- D-0018-2022
- Classification
- Class II
- Product Type
- Drug
- Recalling Firm
- Sanitor Corporation
- Status
- Terminated
- Date Initiated
- 09/21/2021
- Location
- Stanton, CA, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- unknown
Reason for Recall
CGMP Deviations: Use of this product may cause possible infection/ irritation of the skin and/or soft tissues.
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
Distribution Pattern
Distributed to one distributor located in Las Vegas, NV.
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.