---
title: "Maxim Instant Foam Hand Sanitizer (benzalkonium chloride 0.1%) packaged in a)... — FDA record D-1463-2022 | Is It on Recall"
description: "CGMP Deviations: Product manufactured using expired active ingredient, Benzalkonium chloride."
url: https://isitonrecall.com/recall/fda-drug-d-1463-2022-maxim-instant-foam-hand-sanitizer-benzalkonium-chloride-0-1-packaged-in-a-1-u-s-gallon-3-78-liters-d/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA drug enforcement

# Maxim Instant Foam Hand Sanitizer (benzalkonium chloride 0.1%) packaged in a) 1 U.S. Gallon (3.78 Liters) drums UPC 7... — FDA record D-1463-2022

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**: Maxim Instant Foam Hand Sanitizer (benzalkonium chloride 0.1%) packaged in a) 1 U.S. Gallon (3.78 Liters) drums UPC 7 61841 02502 6 and b) 55 U.S. Gallon drums (208 Liters) UPC 0 07 61841 02504 0, Midlab 140 Private Brand Way, Athens, TN 37303
- **Reason**: CGMP Deviations: Product manufactured using expired active ingredient, Benzalkonium chloride.
- **Classification**: Class II
- **Recalling firm**: Midlab Incorporated
- **Quantity**: 892 gallons and one 55-gallon drum
- **Agency-reported status**: Terminated
- **Source record identifier**: D-1463-2022

[Open the official record](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-1463-2022%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 #: a) 03292022-1, 05092022-1, 02012022-1, 06172022-1, 12132021-1, 07272022-1, and b) 06252022-1 |

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-1463-2022%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/)