Humanrace recalls 148mL SPF 30 sunscreen cream that doesn't contain the claimed sun protection level. Consumers should check lot numbers on the bottle for affected batches.
Subpotent Drug: Product does not contain SPF that is declared on the label.
Humanrace is recalling a specific sunscreen product because it doesn't provide the sun protection level it claims. This means users might not get the intended sun protection, increasing the risk of sunburn and skin damage.
The product is labeled as SPF 30 but does not contain the actual sun protection level it claims. This means it may not protect against sunburn as advertised, potentially leading to increased skin damage from sun exposure.
People who own or use the Humanrace Ozone Body Protection Cream SPF 30 in 148mL bottles with specific lot numbers (1752A, 1752B, 1782E, etc.) are affected. Those who rely on this sunscreen for sun protection are most at risk.
Check the bottle for the lot numbers: 1752A, 1752B, 1782E, 1782G, 1782C, 1752C, or 1782B. The product was sold with an expiration date of June 2024.
Look for lot numbers on the bottle: 1752A, 1752B, 1782E, 1782G, 1782C, 1752C, or 1782B.
The product does not contain the claimed sun protection level, so it may not protect against sunburn as advertised. It is not recommended for regular use.
Check the lot numbers on the bottle: 1752A, 1752B, 1782E, 1782G, 1782C, 1752C, or 1782B. The product was sold with an expiration date of June 2024.
The recall does not specify a remedy, so no action is required beyond checking the lot number. Contact Humanrace for more information if needed.
We’ve drafted a message you can send Humanrace to request your refund or repair — edit it as you like.
Subject: Recall D-1176-2023 — Humanrace Humanrace Hello, I own a Humanrace that is covered by recall D-1176-2023 from Humanrace. 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.