---
title: "Avant Foaming Hand Sanitizer Ophardt, Fragrance Free, 1000 mL (33.9 fl. oz.) ... — FDA record D-1356-2022 | Is It on Recall"
description: "CGMP Deviations: product manufactured using deionized water from a system lacking appropriate microbial control post deionization."
url: https://isitonrecall.com/recall/fda-drug-d-1356-2022-avant-foaming-hand-sanitizer-ophardt-fragrance-free-1000-ml-33-9-fl-oz-per-plastic-carton-manufactur/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Avant Foaming Hand Sanitizer Ophardt, Fragrance Free, 1000 mL (33.9 fl. oz.) per plastic carton, Manufactured for B4 ... — FDA record D-1356-2022

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 Jul 15, 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**: Avant Foaming Hand Sanitizer Ophardt, Fragrance Free, 1000 mL (33.9 fl. oz.) per plastic carton, Manufactured for B4 Brands, Lisbon, Iowa 52253
- **Reason**: CGMP Deviations: product manufactured using deionized water from a system lacking appropriate microbial control post deionization.
- **Classification**: Class II
- **Recalling firm**: Aire-Master of America Inc
- **Quantity**: 9,176 cartons
- **Agency-reported status**: Terminated
- **Source record identifier**: D-1356-2022

[Open the official record](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-1356-2022%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 | Product Number 46076 Lot 722896-exp 07/22, 722996-exp 07/22 |

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

## Distribution

Florida, Illinois, Iowa, New Jersey

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

- [Florida](https://isitonrecall.com/state/florida/)
- [Iowa](https://isitonrecall.com/state/iowa/)
- [Illinois](https://isitonrecall.com/state/illinois/)
- [New Jersey](https://isitonrecall.com/state/new-jersey/)

## Dates in the source

- **Report date**: Aug 24, 2022
- **Recall initiation date**: Jul 15, 2022
- **Center classification date**: Aug 18, 2022
- **Termination date**: Feb 19, 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-1356-2022%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/) [Aire-Master of America Inc records](https://isitonrecall.com/brand/aire-master-of-america-inc/)