Agency classClass IIOur severity:High FDA (Drugs)·D-0641-2025·Announced 2025-09-17

Mini sunscreen kits recalled after SPF testing produced inconsistent results

Ultra Violette Mini SPF Mates kits are recalled nationwide after testing of the SPF 50 sunscreen produced inconsistent results ranging from SPF 4 to 64. 44,497 tubes are affected.

The agency’s classification

FDA (Drugs): Class II

Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.

This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work

What this means for you

Our assessment, not the agency’s: severity 3/5 (High).

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: Rubric level 3 covers risk-of-harm products where injury has not yet been reported; a sunscreen that may deliver a fraction of its labeled SPF is a potential harm and no injuries are reported.

Plain-English summary

The Ultra Violette Mini SPF Mates kit, containing Velvet Screen SPF 50 Blurring Mineral SkinScreen with zinc oxide 22.75% and Supreme Sunscreen SPF 50, both in 15 mL (0.5 fl oz) tubes and distributed by Grace & Fire USA Inc., is being recalled. Affected lots are A2453 expiring 11/30/2026 and A2454 expiring 12/31/2026. The recall covers 44,497 tubes distributed nationwide.

The recall was issued because the product is subpotent or superpotent: testing of the SPF 50 sunscreen revealed inconsistency in SPF results ranging from SPF 4, 10, 21, 26, 33, 60, 61 and 64. The FDA classified the action as Class II.

Customers holding these lots should stop relying on the product for sun protection and can return it to the place of purchase.

The recalled product

Product: Ultra Violette Mini SPF Mates kit includes: Velvet Screen SPF 50 Blurring Mineral SkinScreen, Zinc Oxide 22.75%, 15 mL, 0.5 fl. oz. per tube, Supreme Sunscreen SPF 50, 15 mL 0.5 fl. oz. per tube, Distributed by: Grace & Fire USA Inc., 251 Little Falls Drive, New Castle…
Manufacturer: GRACE & FIRE PTY LTD
Category: Drug — Sunscreen
Hazard: subpotency
spf-inconsistency
sunscreen
class-ii
Affected units: 44,497

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (4)

Lot #s: A2453
exp 11/30/2026
A2454
exp 12/31/2026

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 2 recalled by GRACE & FIRE PTY LTD under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 2 products in this recall →

Same manufacturer · GRACE & FIRE PTY LTD

See all →

High
Mineral sunscreen recalled after SPF testing ranged from 4 to 64
FDA (Drugs) · 2025-09-17

Same hazard · subpotency