DrugApr 24, 2019
Estee Lauder Repairwear Laser Focus Line Smoothing Cream Broad Spectrum SPF 15 recall — FDA D-1132-2019
Defective container: Ineffective seal between the cap and jar of the affected product.
Class IIIFDA: TerminatedEstee Lauder Inc.
Recall history in this database
Classification mix: Class III: 2.
DrugFeb 13, 2013
ESTEE LAUDER DayWear Sheer Tint Release, Advanced Multi-Protection Anti-Oxidant Moisturizer recall — FDA D-151-2013
Failed Stability Specifications: The active sunscreen ingredient, avobenzone 3%, may not be stable over the shelf life, the sunscreen effectiveness may be less than labeled.
Class IIIFDA: TerminatedEstee Lauder Inc.
Understanding this recall history
This page summarizes recall records in which the official source identifies Estee Lauder Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.