Home / Recalls / Estee Lauder Inc / D-1132-2019

D-1132-2019 Class III Terminated

Recalled by Estee Lauder Inc — New York, NY

FDA drug recall D-1132-2019 was initiated by Estee Lauder Inc on Mar 15, 2019 and is designated Class III. Reason for recall: Defective container: Ineffective seal between the cap and jar of the affected product. The recall status is terminated (terminated Jan 13, 2025). Affected quantity: 14490 jars.

Recall details

Product Type: Drugs
Report Date: Apr 24, 2019
Initiation Date: Mar 15, 2019
Termination Date: Jan 13, 2025
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 14490 jars

Product description

Repairwear Laser Focus Line Smoothing Cream Broad Spectrum SPF 15, packaged in a light green folding carton containing a 50 mL silver jar with a silver cap, Clinique Laboratories, Dist. New York, NY 10022

Reason for recall

Defective container: Ineffective seal between the cap and jar of the affected product.

Distribution pattern

U.S.A. Nationwide

Code information

Lot #: A68

Source

Dataset: openFDA drug recall enforcement reports
FDA record: This recall in openFDA (JSON)
Enforcement Report: Search FDA's Enforcement Report for D-1132-2019
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.