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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

Silver Star Brands: Various Oral Sprays Recalled for Possible Microbial Contamination

Agency Publication Date: November 2, 2018
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Summary

Approximately 1,640 bottles of Native Remedies and Healthful Naturals oral sprays are being recalled because they may be contaminated with microorganisms. The recall affects six different non-sterile products, including VertiFree, HypoSlim, VaricoGo, EyeClear Pro, DizziFree, and Leg Cramp Support, all sold in 2 fl oz (59 mL) bottles. These items were manufactured by a contract producer under conditions that violated safety standards, potentially allowing harmful bacteria or mold to grow in the products. Consumers who have these sprays should stop using them immediately to avoid health risks.

Risk

The use of products contaminated with microorganisms can lead to serious, potentially life-threatening infections, particularly in individuals with weakened immune systems or when the product is applied to sensitive areas like the eyes or mouth. No specific injuries have been reported, but the manufacturing deviations significantly increase the risk of contamination.

What You Should Do

  1. Check your medicine cabinet for 2 fl oz (59 mL) bottles of Native Remedies or Healthful Naturals oral sprays.
  2. Verify if your product matches these specific identifiers: VertiFree (NDC 68703-253-02, Lot K061417B), HypoSlim (NDC 68703-275-02, Lot K051818A), VaricoGo (NDC 68703-105-59, Lot K111717A), EyeClear Pro (NDC 68703-151-59, Lots K022317A or K022317B), DizziFree (NDC 68703-204-02, Lot K022616D), or Leg Cramp Support (NDC 68703-206-02, Lot K022216C).
  3. Stop using the recalled oral sprays immediately if you identify a matching lot number and NDC code.
  4. Contact your healthcare provider or pharmacist for guidance, especially if you have used the product and feel unwell.
  5. Return any unused product to the place of purchase for a full refund and contact Silver Star Brands for further instructions.
  6. For additional questions, contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA).

Your Remedy Options

💰Full Refund

Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

Affected Products

Product: Native Remedies VertiFree Oral Spray (2 fl oz / 59 mL)
Model:
NDC 68703-253-02
Lot Numbers:
K061417B
Product: Native Remedies HypoSlim Oral Spray (2 fl oz / 59 mL)
Model:
NDC 68703-275-02
Lot Numbers:
K051818A
Product: Native Remedies VaricoGo Oral Spray (2 fl oz / 59 mL)
Model:
NDC 68703-105-59
Lot Numbers:
K111717A
Product: Native Remedies EyeClear Pro Oral Spray (2 fl oz / 59 mL)
Model:
NDC 68703-151-59
Lot Numbers:
K022317A
K022317B
Product: Healthful Naturals DizziFree Oral Spray (2 fl oz / 59 mL)
Model:
NDC 68703-204-02
Lot Numbers:
K022616D
Product: Healthful Naturals Leg Cramp Support Oral Spray (2 fl oz / 59 mL)
Model:
NDC 68703-206-02
Lot Numbers:
K022216C

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 81228
Status: Resolved
Manufacturer: Silver Star Brands
Manufactured In: United States
Units Affected: 6 products (67 bottles; 95 bottles; 53 bottles; 931 bottles; 247 bottles; 247 bottles)
Distributed To: Nationwide
Agency Last Updated: November 19, 2018

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 · 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.