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.
| Brand | GRACE & FIRE PTY LTD |
|---|---|
| Product | Ultra 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. |
| Reason | 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. |
| Severity | moderate |
| Units affected | 44497 |
| Distribution | Nationwide in the USA |
| Agency | FDA |
| Recall / campaign no. | Lot #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 |
WHAT YOU SHOULD DO
- Stop using the recalled product immediately.
- 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.
- Contact Grace & Fire USA Inc. for disposal or refund instructions.
- If you experience a skin reaction, consult a healthcare provider.
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.