Grace & Fire recalls Ultra Violette SPF 50 sunscreen due to inconsistent SPF testing results ranging from SPF 4 to 64. Consumers should check product details and contact the company for guidance.
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.
Grace & Fire is recalling Ultra Violette SPF 50 sunscreen because lab tests showed inconsistent SPF ratings, ranging from SPF 4 to 64. This means the product may not provide the advertised sun protection level, increasing the risk of sunburn and skin damage.
Sunscreen products must provide consistent SPF protection to prevent sunburn and skin damage. Inconsistent SPF results mean the product may not protect as advertised, potentially leading to higher risk of sunburn with prolonged exposure.
Owners of Ultra Violette SPF 50 sunscreen with the specified sizes and lot numbers are affected. People who rely on sunscreen for sun protection are most at risk of inadequate protection.
Check for the product names Ultra Violette, Velvet Screen SPF 50, Blurring Mineral Skinscreen, or Zinc Oxide 22.75%. Look for lot numbers A2455 (15 mL tubes) or A2453A/B, A2454A (50 mL tubes) with expiration dates listed.
Identify the product by checking the lot numbers and expiration dates listed in the recall notice.
The recall is due to inconsistent SPF testing results, but the product may still be safe for use if the user follows the label instructions. However, the product's effectiveness is not guaranteed.
Check the lot numbers: 15 mL tubes with lot A2455 (exp 12/31/2026) or 50 mL tubes with lots A2453A/B, A2454A (exp 11/30/2026 or 12/31/2026).
The recall notice does not specify a remedy, so contact Grace & Fire USA Inc. for further guidance.
We’ve drafted a message you can send Grace & Fire to request your refund or repair — edit it as you like.
Subject: Recall D-0640-2025 — Grace & Fire Grace & Fire Hello, I own a Grace & Fire that is covered by recall D-0640-2025 from Grace & Fire. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
