---
title: "ViaMed Alcohol Prep Pads, For External Use Only, 70% Isopropyl Alcohol, Steri... — FDA record D-0247-2025 | Is It on Recall"
description: "Lack of assurance of sterility and cGMP deviations observed at the manufacturing site."
url: https://isitonrecall.com/recall/fda-drug-d-0247-2025-viamed-alcohol-prep-pads-for-external-use-only-70-isopropyl-alcohol-sterile-100-pieces-per-box-100-b/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# ViaMed Alcohol Prep Pads, For External Use Only, 70% Isopropyl Alcohol, Sterile, 100 pieces per Box, 100 boxes per Ca... — FDA record D-0247-2025

Reported ongoing

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 Feb 12, 2025. 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**: ViaMed Alcohol Prep Pads, For External Use Only, 70% Isopropyl Alcohol, Sterile, 100 pieces per Box, 100 boxes per Carton, Sterile, Manufactured by Wuxi Medical Instrument Factory Co., Ltd., Made in China, Manufactured for: Rece International Corp., Miami Lakes, FL, 33014, USA, NDC: 70006-500-01.
- **Reason**: Lack of assurance of sterility and cGMP deviations observed at the manufacturing site.
- **Classification**: Class II
- **Recalling firm**: Wuxi Medical lnstrument Factory Co., Ltd.
- **Quantity**: 37,500 Boxes
- **Agency-reported status**: Ongoing
- **Source record identifier**: D-0247-2025

[Open the official record](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0247-2025%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 #s: 200830, Exp 08/29/2025; 210925, Exp 09/24/2026; 221225, Exp 12/24/2027. |

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

## Distribution

FL

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/)

## Dates in the source

- **Report date**: Mar 5, 2025
- **Recall initiation date**: Feb 12, 2025
- **Center classification date**: Feb 21, 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-0247-2025%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/) [Wuxi Medical lnstrument Factory Co., Ltd. records](https://isitonrecall.com/brand/wuxi-medical-lnstrument-factory-co-ltd/)