Day Cream SPF15 Cr¿me de jour FPS 15 — Class II drug recall D-0231-2018
Terminated recall by Odan Laboratories Ltd, reported 2018-01-31, distributed nationwide. Failed Stability Specifications:stability failure at 12 months, long term RT conditions.
| Recall number | D-0231-2018 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Odan Laboratories Ltd, Pointe-Claire, N/A, Canada |
| Recall initiated | 2017-12-20 |
| Classified | 2018-01-24 |
| Reported by FDA | 2018-01-31 |
| Terminated | 2018-06-18 |
| Distributed | Nationwide (US) |
| Quantity | 21 jars |
| Reason classes | specification failure |
| UPC / GTIN / UDI-DI | 00626354109550 |
| Lot numbers | J146C |
| Expiration dates | 2019-02 |
Product
Day Cream SPF15 Cr¿me de jour FPS 15, { Avobenzone 2%, Octinoxate 7%, Oxybenzone 5%} 15 ml / 0.5 fl. oz jar. Made in Canada, Kamins Dermatologics Inc. Montreal, Quebec H9R 2Y6. Distributed by Kamins Dermatologics Montreal, Quebec H9R 2Y6 Made in Fabrique au Canada. UPC code 6 26354 10955 0
Reason for recall
Failed Stability Specifications:stability failure at 12 months, long term RT conditions.
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-0231-2018. 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.