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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/Contact Lenses & Vision

Ontact Inc: 24K Premium Lense Contact Lenses Recalled for Potential Bacterial Contamination

Agency Publication Date: July 5, 2024
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Summary

Ontact Inc has recalled 2,842 units of 24K Premium Lense contact lenses, which were distributed by Updream Inc. The recall was initiated because the lenses may be contaminated with bacteria. All distributed lenses under this brand are affected by this recall, which includes products sold in California and Nevada.

Risk

Bacterial contamination in contact lenses poses a serious risk of eye infections, which can lead to permanent vision loss or other severe ocular complications if the contaminated lenses are placed on the eye.

What You Should Do

  1. Check your contact lens packaging for the brand name '24K Premium Lense' distributed by Updream Inc.
  2. Identify if you have any of the 2,842 affected units; the recall applies to all distributed lenses for this specific product.
  3. Immediately stop using the affected contact lenses to prevent the risk of bacterial infection.
  4. Contact your healthcare provider or eye care professional for guidance and to report any eye irritation or signs of infection.
  5. Contact the manufacturer, Ontact Inc, at 10944 Playa Del Sol, Riverside, California, 92503-5243 for further instructions and information regarding a potential refund or replacement.
  6. For additional questions, contact the FDA at 1-888-463-6332 (1-888-INFO-FDA) or visit www.fda.gov/medical-devices/medical-device-recalls.

Your Remedy Options

๐Ÿ“‹Other Action

Manufacturer and Healthcare Consultation

How to: Contact your healthcare provider or the manufacturer for further instructions and potential refund

Affected Products

Product: 24K Premium Lense, Distributed by Updream Inc.
Lot Numbers:
All distributed lenses

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 94692
Status: Active
Manufacturer: Ontact Inc
Sold By: Updream Inc.
Manufactured In: United States
Units Affected: 2,842
Distributed To: California, Nevada

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.