Dry to Normal Skin Starter Kit — Class II drug recall D-0232-2018
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-0232-2018 |
|---|---|
| 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 | 179 kits |
| Reason classes | specification failure |
| Lot numbers | J203, J204, J228, J274 |
| Expiration dates | 2018-02, 2018-09 |
Product
Dry to Normal Skin Starter Kit, Trousse debutante pour peau seche a normale. Kit includes: (Vegetable Cleanser (60 ml / 2 oz), Night Cream (15 g / 0.5 oz), Day Cream SPF15 {Octinoxate 7%, Avobenzone 2% and Oxybenzone 5%} (15 g / 0.5 oz), Eye Cream (6 g / 0.21 oz).Made in Canada, Kamins Dermatologics Inc. Montreal, Quebec H9R 2Y6. Distributed by Kamins Dermatologics (USA) Inc. 99 Hudson, New York, NY, USA. UPC code 6 06354 61322 4
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-0232-2018. 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.