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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Drug
Medications & Supplements/Topical Products

ViaMed Alcohol Prep Pads Recalled for Potential Lack of Sterility

Agency Publication Date: February 21, 2025
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Summary

Wuxi Medical Instrument Factory Co., Ltd. is recalling 37,500 boxes of ViaMed Alcohol Prep Pads (70% Isopropyl Alcohol) because they may not be sterile. The pads were manufactured under conditions that did not meet quality assurance standards, meaning they could contain bacteria. These sterile pads are used by consumers and healthcare providers to clean the skin before an injection or minor medical procedure.

Risk

Using an alcohol pad that is not sterile can introduce bacteria or other contaminants directly into a puncture wound or broken skin, which may lead to serious infections. This risk is highest for patients with weakened immune systems or those who must use these pads for frequent medical injections.

What You Should Do

  1. The recalled products are ViaMed Alcohol Prep Pads (70% Isopropyl Alcohol) sold in boxes of 100 pieces (NDC 70006-500-01). The boxes are labeled as manufactured for Rece International Corp. of Miami Lakes, FL.
  2. Check your supply for lot numbers 200830 (Exp 08/29/2025), 210925 (Exp 09/24/2026), or 221225 (Exp 12/24/2027).
  3. If you have health concerns, contact your healthcare provider or pharmacist. Return any unused product to the place of purchase for a refund, throw it away, or contact Rece International Corp. for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions regarding this recall.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider or pharmacist for guidance, or return any unused product to the place of purchase for a refund
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away. For prescription medications, a DEA take-back location or pharmacy mail-back program is preferred when available.

Affected Products

Product: ViaMed Alcohol Prep Pads (100 pieces per Box)by ViaMed
Variants: 70% Isopropyl Alcohol, External Use Only
Lot Numbers:
200830 (Exp 08/29/2025)
210925 (Exp 09/24/2026)
221225 (Exp 12/24/2027)
NDC:
70006-500-01

Manufactured by Wuxi Medical Instrument Factory Co., Ltd.; Distributed by Rece International Corp.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 96210
Status: Active
Manufacturer: Wuxi Medical lnstrument Factory Co., Ltd.
Sold By: Rece International Corp.
Manufactured In: China
Units Affected: 37,500 Boxes
Distributed To: Florida

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.