---
title: "Allergy Bee Gone for Kids Nasal Swab Remedy 0.33 FL OZ (10 mL) tubes, UPC Cod... — FDA record D-1160-2022 | Is It on Recall"
description: "Microbial contamination of non-sterile product: FDA laboratory analysis found product to contain elevated levels of yeast and mold as well as the presence of Ba"
url: https://isitonrecall.com/recall/fda-drug-d-1160-2022-allergy-bee-gone-for-kids-nasal-swab-remedy-0-33-fl-oz-10-ml-tubes-upc-code-860002022116/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Allergy Bee Gone for Kids Nasal Swab Remedy 0.33 FL OZ (10 mL) tubes, UPC Code 860002022116 — FDA record D-1160-2022

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 Jun 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**: Allergy Bee Gone for Kids Nasal Swab Remedy 0.33 FL OZ (10 mL) tubes, UPC Code 860002022116
- **Reason**: Microbial contamination of non-sterile product: FDA laboratory analysis found product to contain elevated levels of yeast and mold as well as the presence of Bacillus cereus.
- **Classification**: Class I
- **Recalling firm**: Buzzagogo, LLC
- **Quantity**: 28,328 tubes
- **Agency-reported status**: Terminated
- **Source record identifier**: D-1160-2022

[Open the official record](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-1160-2022%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 #: 2006491, Exp. Date 08/24 |

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

## Distribution

Product was distributed via the internet to consumers, retailers and to distributors who may have further distributed the product.

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Jul 6, 2022
- **Recall initiation date**: Jun 8, 2022
- **Center classification date**: Jun 24, 2022
- **Termination date**: Sep 26, 2022

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-1160-2022%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/) [Buzzagogo, LLC records](https://isitonrecall.com/brand/buzzagogo-llc/)