Recall archive / FDA drug enforcement
Corsair Personal Care 99X Instant Foam Hand Sanitizer (benzalkonium chloride 0.1%)128 Fl. Oz. (1 Gal.) 3.78 liters bo... — FDA record D-1464-2022
Reported terminated
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Aug 8, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- 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
- CGMP Deviations: Product manufactured using expired active ingredient, Benzalkonium chloride.
- Classification
- Class II
- Recalling firm
- Midlab Incorporated
- Quantity
- Not supplied
- Agency-reported status
- Terminated
- Source record identifier
- D-1464-2022
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | Lot #: 06172022-1 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
Naionwide within the United States
No US distribution state could be established from this record. Check the official notice.
Dates in the source
- Report date
- Aug 31, 2022
- Recall initiation date
- Aug 8, 2022
- Center classification date
- Aug 25, 2022
- Termination date
- Aug 15, 2023
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.