Estee Lauder Inc

FDA recalling firm · 3 enforcement events · 3 product records · 2012–2019 · NY

Estee Lauder Inc has 3 FDA enforcement events on this register (3 product records) between 2012 and 2019: 3 drug; the busiest year was 2012 with 1.

0% of its events are Class I; the most common class is Class III (3). 0 events are listed as ongoing; the recalling firm's address is in NY.

Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.

Enforcement events

Initiated	Product (first record)	Type	Class	Records	Status
15 Mar 2019	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	Drug	Class III	1	Terminated
6 Jun 2014	DENBLAN Anticavity Fluoride Toothpaste, Whitening formula, sodium monofluorophosphate 0.76%, 2.6 oz/75 mL tube, Laboratories Darphin, Dist, Paris France	Drug	Class III	1	Terminated
23 Oct 2012	ESTEE LAUDER DayWear Sheer Tint Release, Advanced Multi-Protection Anti-Oxidant Moisturizer Broad Spectrum SPF15, All Skin types, 1.7 FL. OZ. LIQ/50 ml (tube inside a unit carton) with UPC No. 2713179904, Code WKEM-01, and 1.5 mL foil sample packets, ESTEE LAUDER, DIST., NEW YORK, N.Y. 10022 NDC 11559-008-01	Drug	Class III	1	Terminated

By type and class

Drug3

Class III3

Class I: 0% of this firm's events; 18% of all events on the register.

Events by year

Enforcement events for Estee Lauder Inc by year initiated.

Questions and answers

How many FDA recalls has Estee Lauder Inc had?

3 enforcement events (3 product records) on this register, 2012–2019: 3 drug.

Are any Estee Lauder Inc recalls ongoing?

0 events are listed as ongoing in the current openFDA export.

What class are Estee Lauder Inc recalls?

3 Class III. 0% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.

Where does this data come from?

openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.

Provenance

Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.