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Ultra Violette Mini SPF Mates kit includes: Velvet Screen SPF 50 Blurring Mineral SkinScre… recall

FDA recall D-0641-2025 · initiated Aug 22, 2025

By the pharmaranks editorial teamReviewed against the FDA (openFDA) sourcesUpdated Sep 17, 2025How we research

GRACE & FIRE PTY LTD recalled Ultra Violette Mini SPF Mates kit includes: Velvet Screen SPF 50 Blurring Minera… in Aug 2025 — an FDA Class II recall (D-0641-2025) because 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.

May cause temporary or medically reversible harm; low probability of serious harm.

Why it was recalled

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.

Wrong strength, or it did not keep

The product did not contain what the label promised, or stopped meeting specification before its expiry date. Under-strength medicine can mean an untreated condition.

This is a manufacturing or quality failure, not a finding that the medicine is unsafe to take — across every recall we hold, none was issued for that reason. It does not mean the batch was harmless.

Is your product affected? Check the lot number

A recall covers only specific lots. Find the lot number and expiration date on your package and compare them to the affected codes below — if yours is not listed, it was not part of this recall.

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

Quantity recalled: 44,497 tubes

Details

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 Wilmington, Delaware 19808, NDC 84803-110-01 (15 mL Velvet Screen), UPC 9355909005757.
Recalling company
GRACE & FIRE PTY LTD
Classification
Class II
Status
Ongoing
Type
Voluntary: Firm initiated
Distribution
Nationwide in the USA
Initiated
Aug 22, 2025
FDA report date
Sep 17, 2025
What to do.If you have a recalled product, don't throw away questions — check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This page reproduces public FDA data and is not medical advice.

Frequently asked

Was Ultra Violette Mini SPF Mates kit includes: Velvet Screen SPF 50 Blurring Minera… recalled?
GRACE & FIRE PTY LTD recalled Ultra Violette Mini SPF Mates kit includes: Velvet Screen SPF 50 Blurring Minera… in Aug 2025 — an FDA Class II recall (D-0641-2025) because 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. May cause temporary or medically reversible harm; low probability of serious harm.
Why was Ultra Violette Mini SPF Mates kit includes: Velvet Screen SPF 50 Blurring Minera… recalled?
Per the FDA enforcement record, the reason for recall D-0641-2025 was: 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.
Is a recalled Ultra Violette Mini SPF Mates kit includes: Velvet Screen SPF 50 Blurring Minera… dangerous to take?
An FDA recall removes specific lots from the market for a defined reason and does not by itself mean the medicine is unsafe for everyone — your specific lot may never have been affected. May cause temporary or medically reversible harm; low probability of serious harm. Check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This reproduces public FDA data and is not medical advice.
Which lots of Ultra Violette Mini SPF Mates kit includes: Velvet Screen SPF 50 Blurring Minera… are affected?
Distributed: Nationwide in the USA. The recall covers these lots — Lot #s: A2453, exp 11/30/2026; A2454, exp 12/31/2026. Check the lot number and expiration date on your package against this list; if yours is not listed, it was not part of recall D-0641-2025.

Source: openFDA Drug Enforcement record D-0641-2025

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