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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/Topical Products

La Fresh Group, Inc.: Sunnyside Lotion Wipes Recalled for Marketing as an Unapproved Sunscreen

Agency Publication Date: July 22, 2019
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Summary

La Fresh Group, Inc. is recalling approximately 83,050 Travel Lite Sunnyside Lotion Wipes because they were marketed without proper FDA approval as a sunscreen. The product's labeling and online descriptions include claims about sun protection that have not been vetted for safety or effectiveness through the required New Drug Application (NDA) process. These wipes were sold individually in 4.75" x 5.75" packets on the firm's website and Amazon.com. Consumers should not rely on this product for sun protection and should contact a healthcare provider for guidance on appropriate sunscreen use.

Risk

The product claims to provide sun protection but has not been approved by the FDA for such use, meaning its safety and effectiveness as a sunscreen are unverified. Relying on an unproven product for sun protection may lead to inadequate protection against ultraviolet (UV) radiation, potentially resulting in sunburns or increased long-term skin damage.

What You Should Do

  1. Check your individual 4.75" x 5.75" Sunnyside Lotion Wipe packets for the recall number D-1566-2019 and lot numbers beginning with 453091.
  2. Immediately stop using the product for sun protection purposes.
  3. Contact your healthcare provider or pharmacist for guidance regarding any skin concerns or for recommendations on approved sunscreen products.
  4. Return any unused product to the place of purchase for a refund and contact La Fresh Group, Inc. at 1-909-591-6100 or through their website at www.LaFreshGroup.com for further instructions.
  5. For additional questions, contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls.

Your Remedy Options

๐Ÿ’ฐFull Refund

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

How to: Return the product to the place of purchase for a refund and seek medical advice for sun protection alternatives.

Affected Products

Product: LA FRESH travel lite Sunnyside Lotion Wipe (1 individually wrapped packet)
Model:
D-1566-2019
Lot Numbers:
All lots beginning with 453091

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 82857
Status: Resolved
Manufacturer: La Fresh Group, Inc.
Sold By: Amazon.com; LaFreshGroup.com
Manufactured In: United States
Units Affected: 83,050 packets
Distributed To: Nationwide
Agency Last Updated: July 31, 2019

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.