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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
Personal Care & Cosmetics/Skincare

Ultra Violette Velvet Screen SPF 50 Sunscreen Recalled for SPF Inconsistency

Agency Publication Date: September 11, 2025
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Summary

Grace & Fire PTY LTD is recalling approximately 93,772 tubes of Ultra Violette Velvet Screen SPF 50 and Mini SPF Mates kits because testing revealed the sun protection factor (SPF) is inconsistent. While labeled as SPF 50, test results varied wildly from as low as SPF 4 to as high as SPF 64. The affected products were distributed nationwide in the USA and include both 15 mL and 50 mL tubes.

Risk

The product may provide significantly less sun protection than the SPF 50 labeled on the package, which increases the risk of sunburn and long-term skin damage from UV radiation. For users who may be over-exposed to the sun thinking they are protected, this could lead to serious skin irritation or burns.

What You Should Do

  1. Check your sunscreen packaging for 'Ultra Violette Velvet Screen SPF 50' or the 'Mini SPF Mates' kit to see if your product is affected.
  2. Check the lot number and expiration date printed on your tube or kit box. See the Affected Products section below for the full list of affected codes.
  3. If you have health concerns or have experienced skin issues after using these products, contact your healthcare provider or pharmacist.
  4. Return any unused product to the place of purchase for a refund, throw it away, or contact Grace & Fire USA 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:

๐Ÿ’ฐOption 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
๐Ÿ—‘๏ธ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: Ultra Violette, Velvet Screen SPF 50, Blurring Mineral Skinscreen (15 mL)by Ultra Violette
Variants: 15 mL (0.5 fl. oz.) tube, Zinc Oxide 22.75%
UPC Codes:
9355909006068
Lot Numbers:
A2455 (Exp 12/31/2026)
NDC:
84803-106-01

Distributed by Grace & Fire USA Inc.

Product: Ultra Violette, Velvet Screen SPF 50, Blurring Mineral Skinscreen (50 mL)by Ultra Violette
Variants: 50 mL (1.7 fl. oz.) tube, Zinc Oxide 22.75%
UPC Codes:
9355909005924
Lot Numbers:
A2453A (Exp 11/30/2026)
A2453B (Exp 11/30/2026)
A2454A (Exp 12/31/2026)
A2550 (Exp 02/28/2027)
NDC:
84803-106-02

Distributed by Grace & Fire USA Inc.

Product: Ultra Violette Mini SPF Mates kitby Ultra Violette
Variants: Includes 15 mL Velvet Screen SPF 50 and 15 mL Supreme Sunscreen SPF 50
UPC Codes:
9355909005757
Lot Numbers:
A2453 (Exp 11/30/2026)
A2454 (Exp 12/31/2026)
NDC:
84803-110-01

Distributed by Grace & Fire USA Inc.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 97498
Status: Active
Manufacturer: GRACE & FIRE PTY LTD
Sold By: Grace & Fire USA Inc.
Manufactured In: Australia
Units Affected: 2 products (49,275 tubes; 44,497 tubes)
Distributed To: Nationwide

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.