Home / Recalls / Estee Lauder Inc / D-1452-2014

D-1452-2014 Class III Terminated

Recalled by Estee Lauder Inc — New York, NY

FDA drug recall D-1452-2014 was initiated by Estee Lauder Inc on Jun 6, 2014 and is designated Class III. Reason for recall: Stability Data Does Not Support Expiry The recall status is terminated (terminated Nov 19, 2015). Affected quantity: 3,791 tubes.

Recall details

Product Type: Drugs
Report Date: Jul 30, 2014
Initiation Date: Jun 6, 2014
Termination Date: Nov 19, 2015
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 3,791 tubes

Product description

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

Distribution pattern

Nationwide

Code information

All lot codes and shipment dates are being recalled. 2.6oz/75ml. in a light green carton, UPC: 8-82381-07901-7 Code: D079-01-1000

Source

Dataset: openFDA drug recall enforcement reports
FDA record: This recall in openFDA (JSON)
Enforcement Report: Search FDA's Enforcement Report for D-1452-2014
openFDA file date: Nov 10, 2026
Loaded by RegDataLab: Nov 11, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.