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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/Over-the-Counter

Spectrum Advanced Gel Hand Sanitizer Recalled for Low Alcohol Content

Agency Publication Date: June 5, 2025
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Summary

Consumer Product Partners, LLC is recalling 125,040 bottles of Spectrum Advanced Gel Hand Sanitizer (Ethyl Alcohol 70%) because the product tested below the required alcohol level and may appear cloudy. The recall affects 8 FL OZ (236 mL) bottles manufactured for Medline Industries, Inc. and distributed nationwide in the United States. Consumers should stop using the affected sanitizer, as it does not meet the potency standards for killing germs as labeled.

Risk

The product is subpotent, meaning it contains less than the 70% ethyl alcohol concentration required for effective hand hygiene. This failure to meet potency standards may leave users unprotected against bacteria and viruses, increasing the risk of infection.

What You Should Do

  1. The recalled product is Spectrum Advanced Gel Hand Sanitizer (Ethyl alcohol 70%) sold in 8 FL OZ (236 mL) bottles with UPC 8 88277 34945 5 and NDC 53329-202-08. Only Lot 0644682 (exp 2026/11/14) and Lot 0644683 (exp 2026/11/16) are included in this recall.
  2. 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 the manufacturer for further instructions.
  3. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional assistance or visit www.fda.gov/safety/recalls.

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: Spectrum Advanced Gel Hand Sanitizer (8 FL OZ)
Variants: Ethyl alcohol 70%, 8 FL OZ (236 mL)
UPC Codes:
888277349455
Lot Numbers:
0644682 (Exp 2026/11/14)
0644683 (Exp 2026/11/16)
NDC:
53329-202-08

Manufactured for Medline Industries, Inc.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 96960
Status: Active
Manufacturer: Consumer Product Partners, LLC
Sold By: Medline Industries, Inc.
Manufactured In: United States
Units Affected: 125,040 bottles
Distributed To: Nationwide

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.