HIGHFDA DRUG

Ultra Violette Mini Mates SPF 50 Kit Recalled for SPF Variability in 44,497 Tubes (2025)

Ultra Violette Mini Mates SPF 50 kit sold nationwide in the U.S. is recalled. Testing showed SPF results ranging from 4 to 64. The recall is issued by Grace & Fire USA Inc. The public was notified by letter.

Official notice

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DRUG
Recall date
August 22, 2025
Status
ACTIVE
Severity
8/10

Quick Facts at a Glance

Recall Date
August 22, 2025
Hazard Level
HIGH
Brands
ULTRA VIOLETTE MINI MATES, Grace And Fire USA Inc.
Category
Health & Personal Care
Sold At
Unknown
Geographic Scope
1 states
At-Risk Groups
GENERAL, PREGNANT, PETS

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Drug Safety; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
ULTRA VIOLETTE MINI MATES, Grace And Fire USA Inc.
Product type
Sunscreen SPF 50 kit
Model numbers
A2453, A2454
UPC codes
84803-110, 84803-110-01, 84803-106-01, 84803-100-15, 9355909005
Sizes
15 mL (0.5 fl oz) per tube
Sold at
Unknown
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    August 22, 2025

  2. Reported by FDA DRUG

    September 17, 2025

  3. RecallRadar source check

    April 18, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

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

About This Product

The kit bundles two SPF 50 sunscreen products. Consumers buy SPF products for sun protection during outdoor activities.

Why This Is Dangerous

Inconsistent SPF means unpredictable protection, potentially leading to sunburn or overexposure depending on the applied amount.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

Consumers may be exposed to higher sunburn risk or misleading protection levels.

Practical Guidance

How to identify if yours is affected

  1. Check model numbers on the packaging (A2453, A2454).
  2. Inspect NDC 84803-110-01 and UPC 9355909005757 on the tube.
  3. Confirm kit includes Velvet Screen SPF 50 and Supreme Sunscreen SPF 50.

Where to find product info

FDA enforcement page and recall notice for D-0641-2025.

What timeline to expect

Refunds or replacements will follow recall notification letters; no specific timeframe provided.

If the manufacturer is unresponsive

  • Document all correspondence.
  • Escalate to consumer protection agencies if no response after 4-6 weeks.

How to prevent similar issues

  • Avoid SPF products with unclear potency testing.
  • Prefer products with consistent SPF test results across batches.
  • Verify NDC/UPC and model numbers before purchase.

Documentation advice

Keep packaging, receipts, and recall notices; photograph lot codes and serial numbers.

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Product Details

Product: Ultra Violette Mini Mates SPF 50 kit. Models: A2453, A2454. Distributor: Grace & Fire USA Inc., 251 Little Falls Drive, New Castle Wilmington, DE 19808. Quantity: 44,497 tubes. Distribution: Nationwide in the USA. NDC: 84803-110-01 (15 mL Velvet Screen). UPC: 9355909005757. Sold as kit and included items Velvet Screen SPF 50 Blurring Mineral SkinScreen and Supreme Sunscreen SPF 50. Recall date: 2025-08-22. Recall status: ACTIVE.

Reported Incidents

No specific injuries or incidents are described in the provided data. The recall status is Class II with high hazard level due to SPF inconsistency.

Key Facts

  • Models A2453 and A2454
  • Recall Date 2025-08-22 (ACTIVE)

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERALPREGNANTPETS
Injury Types
BURNOTHER

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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