HIGH

Ultra Violette Mini SPF Sunscreen Kit Recalled Over Inconsistent SPF Levels

Ultra Violette recalled 44,497 tubes of its Mini SPF Mates kit on August 22, 2025. The sunscreen products showed inconsistent SPF results, including readings as low as SPF 4. Consumers must stop use immediately and contact the distributor for guidance.

Hazard Information

Subpotent/Super-potent Product: Testing of the SPF 50 sunscreen revealed inconsistency in SPF results ranging from SPF 4, 10, 21, 26, 33, 60, 61, and 64.

What You Should Do

Consumers and healthcare providers should stop using this product immediately. Contact GRACE & FIRE PTY LTD or your healthcare provider for guidance. Notification method: Letter

Product Details

The recalled product is the Ultra Violette Mini SPF Mates kit, which includes Velvet Screen SPF 50 and Supreme Sunscreen SPF 50. The products were distributed by Grace & Fire USA Inc. The lot numbers affected are A2453 and A2454, with expiration dates of November 30, 2026, and December 31, 2026.

The Hazard

Testing revealed the SPF 50 sunscreen's effectiveness varied greatly, with some tests showing SPF levels as low as 4. This inconsistency poses a significant risk to consumers relying on these products for sun protection.

Reported Incidents

There are no reported injuries or incidents associated with the recalled products at this time. However, the potential for inadequate sun protection is a serious concern.

What to Do

Consumers should stop using the affected products immediately. For further guidance, contact GRACE & FIRE PTY LTD or consult your healthcare provider.

Contact Information

For more information, visit the FDA website at https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=D-0641-2025. Consumers can also reach out to the distributor for assistance.

Key Facts

  • 44,497 tubes recalled
  • Inconsistent SPF results ranging from SPF 4 to 64
  • Distributed nationwide in the USA
  • Stop using the product immediately
  • Contact GRACE & FIRE PTY LTD for guidance
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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product Details

Model Numbers
A2453
A2454
UPC Codes
84803-110
84803-110-01
84803-106-01
+2 more
Affected States
ALL
Report Date
September 17, 2025
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE
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