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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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Critical RiskFDA Drug
Medications & Supplements/Over-the-Counter

SnoreStop NasoSpray Recalled for Microbial Contamination

Agency Publication Date: June 27, 2022
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Summary

Green Pharmaceuticals, Inc. is recalling 1,074 bottles of SnoreStop NasoSpray, a homeopathic nasal spray. This recall was issued after FDA testing found microbial contamination identified as Providencia rettgeri in the product. The affected spray bottles are 0.3 FL OZ (9 mL) in size.

Risk

The use of a nasal spray contaminated with Providencia rettgeri can lead to serious infections, especially in individuals with compromised immune systems or those who have existing nasal injuries.

What You Should Do

  1. This recall affects SnoreStop NasoSpray (0.3 FL OZ / 9 mL) with UPC 769682291013 and NDC 61152-199-99.
  2. Check your product for Lot # 2373/21222, which is printed on the label of the spray bottle.
  3. If you have health concerns after using this product, contact your healthcare provider or pharmacist.
  4. Return any unused product to the place of purchase for a refund, throw it away, or contact Green Pharmaceuticals, Inc. for further instructions.
  5. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions.

Your Remedy Options

You have 2 options:

💰Option 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
🗑️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: SnoreStop NasoSpray (0.3 FL OZ)by SnoreStop
Variants: 0.3 FL OZ, 9 mL
UPC Codes:
769682291013
Lot Numbers:
2373/21222
NDC:
61152-199-99

Homeopathic Anti-Snoring Nasal Spray

Product Images

“Product front image, SnoreStop NasoSpray”

“Product front image, SnoreStop NasoSpray”

“Product back image, SnoreStop NasoSpray”

“Product back image, SnoreStop NasoSpray”

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 90384
Status: Resolved
Manufacturer: Green Pharmaceuticals, Inc.
Manufactured In: United States
Units Affected: 1074 spray bottles
Distributed To: Nationwide
Agency Last Updated: July 7, 2022

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 · FDA Press Release · 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.