RECALL DATABASE

Sunscreen Recall: Ultra Violette Velvet Screen SPF 50

Announced 2025-09-17 · FDA

The FDA is recalling Ultra Violette Velvet Screen SPF 50 Blurring Mineral SkinScreen due to inconsistent SPF test results ranging from SPF 4 to 64. About 49,275 tubes distributed nationwide in the USA are affected. No corrective action is listed.

BrandGRACE & FIRE PTY LTD
ProductUltra Violette, Velvet Screen SPF 50, Blurring Mineral Skinscreen, Zinc Oxide 22.75%, a) 15 mL, 0.5 fl. oz. per tube, NDC 84803-106-01, UPC 9355909006068, b) 50 mL, 1.7 fl. oz. per tube, NDC 84803-106-02, UPC 9355909005924, Distributed by: Grace & Fire USA Inc., 251 Little Falls Drive, New Castle Wilmington, Delaware 19808.
ReasonSubpotent/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.
Severitymoderate
Units affected44497
DistributionNationwide in the USA
AgencyFDA

WHAT YOU SHOULD DO

  1. Stop using the recalled product immediately.
  2. Check the tube for the listed lot numbers (A2455 for 15 mL; A2453A, A2453B, A2454A, A2550 for 50 mL) and expiration dates; discard any affected tubes.
  3. Contact Grace & Fire USA Inc. for disposal or refund instructions.
  4. If you experience a skin reaction, consult a healthcare provider.

How to identify the recalled item

Lot / date codesLot #s: a) 15 mL tubes: A2455, exp 12/31/2026; b) 50 mL tubes: A2453A, A2453B, exp 11/30/2026; A2454A, exp 12/31/2026; A2550, exp 02/28/2027
Lot / date codesLot #s: A2453, exp 11/30/2026; A2454, exp 12/31/2026

These are the identifiers FDA published for this recall. Most recall notices list no UPC or model number at all — if the code on your item is not shown here, that does not mean the item is excluded. Check the official notice, or contact the company.

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This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.