---
title: "FOAMING HAND SANITIZER, fresh mint scent, 62% alcohol, 1 Gallon / 3.78 Liters... — FDA record D-0760-2023 | Is It on Recall"
description: "CGMP Deviations: FDA analysis found product to contain acetaldehyde and acetal above specification limits."
url: https://isitonrecall.com/recall/fda-drug-d-0760-2023-foaming-hand-sanitizer-fresh-mint-scent-62-alcohol-1-gallon-3-78-liters-bottle-290-alpha-drive-ridc/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# FOAMING HAND SANITIZER, fresh mint scent, 62% alcohol, 1 Gallon / 3.78 Liters bottle, 290 Alpha Drive RIDC industrial... — FDA record D-0760-2023

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 May 16, 2023. 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**: FOAMING HAND SANITIZER, fresh mint scent, 62% alcohol, 1 Gallon / 3.78 Liters bottle, 290 Alpha Drive RIDC industrial Park, Pittsburgh, PA 15238,
- **Reason**: CGMP Deviations: FDA analysis found product to contain acetaldehyde and acetal above specification limits.
- **Classification**: Class II
- **Recalling firm**: Alpha Aromatics
- **Quantity**: 544 1 gallon bottles
- **Agency-reported status**: Terminated
- **Source record identifier**: D-0760-2023

[Open the official record](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0760-2023%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: 2020-013211 and 2020-013629, No EXP date on label. |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

Product was distributed to one account in NC.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [North Carolina](https://isitonrecall.com/state/north-carolina/)

## Dates in the source

- **Report date**: May 31, 2023
- **Recall initiation date**: May 16, 2023
- **Center classification date**: May 22, 2023
- **Termination date**: Jul 1, 2024

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-0760-2023%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/) [Alpha Aromatics records](https://isitonrecall.com/brand/alpha-aromatics/)