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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 Device
Medical Devices/Home Healthcare

NeilMed NasoGel Spray Recalled for Potential Bacterial Growth

Agency Publication Date: February 5, 2025
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Summary

Neilmed Pharmaceuticals Inc. has voluntarily recalled approximately 89,312 units of NeilMed NasoGel for DRY NOSES. This saline-based gel spray, used to moisturize irritated nasal passages, was found to have stability issues that could lead to the growth of bacteria (bioburden). While no injuries or infections have been reported to date, the manufacturer initiated the recall after discovery of the failure.

Risk

The product may contain bacterial growth that exceeds safety standards. Using contaminated nasal spray can lead to infections, which pose a higher risk to individuals with compromised immune systems or those who have recently undergone nasal surgery or experienced nasal trauma.

What You Should Do

  1. The recalled product is NeilMed NasoGel for DRY NOSES, a saline-based gel spray sold in bottles with UPC 00705928045309.
  2. Check the packaging for the following affected lot numbers: NGS751, NGS754, NGS755, NGS756, NGS757, NGS760, NGS761, or NGS762.
  3. Identify your specific product by checking for SKUs GSP30-2R-48-ENU-USL, GSP30-0R-96-ENU-USL, GSP30-ARA-INTL, GSP30-SWE-INTL, GSP30-ENG-INT, GSP30-MAL-INTL, or GSP30-SPA-INT.
  4. Stop using the product. Return it to the place of purchase for a refund or replacement, throw it away, or contact your healthcare provider or Neilmed Pharmaceuticals Inc. for further instructions.
  5. Call the FDA Consumer Complaint hotline at 1-888-463-6332 for additional information regarding this recall.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider, or return the product to the place of purchase for a refund or replacement
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Stop using and throw the product away.

Affected Products

Product: NeilMed NasoGel for DRY NOSES
Model / REF:
GSP30-2R-48-ENU-USL
GSP30-0R-96-ENU-USL
GSP30-ARA-INTL
GSP30-SWE-INTL
GSP30-ENG-INT
GSP30-MAL-INTL
GSP30-SPA-INT
Lot Numbers:
NGS751
NGS757
NGS762
NGS754
NGS755
NGS756
NGS760
NGS761
UDI:
00705928045309
GTIN:
00705928045309

NasoGel Spray is a saline-based gel formula used to moisturize and lubricate dry and irritated nasal passages.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 96076
Status: Active
Manufacturer: Neilmed Pharmaceuticals Inc
Sold By: Nationwide retailers; International distributors
Manufactured In: United States
Units Affected: 89,312
Distributed To: Alabama, Arizona, California, Colorado, Connecticut, Florida, Georgia, Idaho, Illinois, Indiana, Kentucky, Massachusetts, Maryland, Michigan, Minnesota, Missouri, North Carolina, New Jersey, New Mexico, New York, Ohio, Oregon, Pennsylvania, Rhode Island, South Carolina, Tennessee, Texas, Virginia, Vermont, Washington, Wisconsin
Agency Last Updated: February 7, 2025

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.