D-1464-2022 Class II Terminated
FDA drug recall D-1464-2022 was initiated by Midlab Incorporated on August 8, 2022 and is designated Class II. Reason for recall: CGMP Deviations: Product manufactured using expired active ingredient, Benzalkonium chloride. The recall status is terminated (terminated August 15, 2023).
Recall Details
- Product Type
- Drugs
- Report Date
- August 31, 2022
- Initiation Date
- August 8, 2022
- Termination Date
- August 15, 2023
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
Product Description
Corsair Personal Care 99X Instant Foam Hand Sanitizer (benzalkonium chloride 0.1%)128 Fl. Oz. (1 Gal.) 3.78 liters bottles, Southern Products & Services, Inc. 2515 Jake Drive Ste B, Cumming, GA 30028
Reason for Recall
CGMP Deviations: Product manufactured using expired active ingredient, Benzalkonium chloride.
Distribution Pattern
Naionwide within the United States
Code Information
Lot #: 06172022-1