---
title: "Little Remedies Gas Relief Drops (Simethicone/Antigas), packaged in 1 fl. oz.... — FDA record D-0557-2024 | Is It on Recall"
description: "cGMP deviations: Test results confirmed aypical Burkholderia Cepacia were a result of personnel error."
url: https://isitonrecall.com/recall/fda-drug-d-0557-2024-little-remedies-gas-relief-drops-simethicone-antigas-packaged-in-1-fl-oz-30-ml-bottle-with-dropper-d/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Little Remedies Gas Relief Drops (Simethicone/Antigas), packaged in 1 fl. oz. (30 mL) bottle with dropper, Dist by Me... — FDA record D-0557-2024

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 28, 2024. 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**: Little Remedies Gas Relief Drops (Simethicone/Antigas), packaged in 1 fl. oz. (30 mL) bottle with dropper, Dist by Medtech Products Inc., Tarrytown, NY 10591, NDC 63029-103-02
- **Reason**: cGMP deviations: Test results confirmed aypical Burkholderia Cepacia were a result of personnel error.
- **Classification**: Class II
- **Recalling firm**: Denison Pharmaceuticals, LLC
- **Quantity**: 113,544 bottles
- **Agency-reported status**: Terminated
- **Source record identifier**: D-0557-2024

[Open the official record](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0557-2024%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 #: 0855, Exp. 8/31/ 2025 |

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

## Distribution

Recalled units were distributed to one customer. 100% recovered (113,544 units) and controlled at Denison Pharmaceuticals.

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

## Dates in the source

- **Report date**: Jun 26, 2024
- **Recall initiation date**: May 28, 2024
- **Center classification date**: Jun 17, 2024
- **Termination date**: Aug 26, 2025

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-0557-2024%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/) [Denison Pharmaceuticals, LLC records](https://isitonrecall.com/brand/denison-pharmaceuticals-llc/)