DENBLAN Anticavity Fluoride Toothpaste — Class III drug recall D-1452-2014
Terminated recall by Estee Lauder Inc, reported 2014-07-30, distributed nationwide. Stability Data Does Not Support Expiry
| Recall number | D-1452-2014 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Estee Lauder Inc, New York, NY, United States |
| Recall initiated | 2014-06-06 |
| Classified | 2014-07-24 |
| Reported by FDA | 2014-07-30 |
| Terminated | 2015-11-19 |
| Distributed | Nationwide (US) |
| Quantity | 3,791 tubes |
| Reason classes | specification failure |
| UPC / GTIN / UDI-DI | 00882381079017 |
Product
DENBLAN Anticavity Fluoride Toothpaste, Whitening formula, sodium monofluorophosphate 0.76%, 2.6 oz/75 mL tube, Laboratories Darphin, Dist, Paris France
Reason for recall
Stability Data Does Not Support Expiry
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-1452-2014. 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.