Humanrace Suncare — Class II drug recall D-1176-2023
Ongoing recall by HUMANRACE, reported 2023-09-27, distributed nationwide. Subpotent Drug: Product does not contain SPF that is declared on the label.
| Recall number | D-1176-2023 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | HUMANRACE, Beverly Hills, CA, United States |
| Recall initiated | 2023-08-18 |
| Classified | 2023-09-21 |
| Reported by FDA | 2023-09-27 |
| Distributed | Nationwide (US) |
| Countries outside the US | ES, FR, GB, IT |
| Quantity | 2,942 units |
| Reason classes | labeling, potency |
| Lot numbers | 1752A, 1752B, 1752C, 1782B, 1782C, 1782E, 1782G |
| Expiration dates | 2024-06 |
Product
Humanrace Suncare, Ozone Body Protection Cream, Broad Spectrum Sunscreen SPF 30, packaged as a 148mL (5 fl oz.) bottle, PA ++++, 100% mineral, Active Ingredient: Zinc oxide 15%, Snow Mushroom, Squalene, Aloe, Dist. By: @Humanrace 2022 Beverly Hills, CA 90210, USA, NDC 82779-002
Reason for recall
Subpotent Drug: Product does not contain SPF that is declared on the label.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1176-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.