---
title: "Corsair Personal Care 99X Instant Foam Hand Sanitizer (benzalkonium chloride ... — FDA record D-1464-2022 | Is It on Recall"
description: "CGMP Deviations: Product manufactured using expired active ingredient, Benzalkonium chloride."
url: https://isitonrecall.com/recall/fda-drug-d-1464-2022-corsair-personal-care-99x-instant-foam-hand-sanitizer-benzalkonium-chloride-0-1-128-fl-oz-1-gal-3-78/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / 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](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## 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

[Open the official record](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-1464-2022%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). 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.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-1464-2022%22)

## Before changing a medicine

Follow urgent instructions in the current official recall notice. Speak to your pharmacist or prescriber before stopping or changing a prescribed medicine.

Talk to your doctor or pharmacist if you have questions or concerns about your medicine. [FDA medication recall guidance](https://www.fda.gov/drugs/drug-recalls/understanding-drug-recalls-what-know-and-what-do)

## Related records

[Medications records](https://isitonrecall.com/category/medications/) [Midlab Incorporated records](https://isitonrecall.com/brand/midlab-incorporated/)