The Recall Desk

Manufacturer

Estee Lauder Inc

3 recalls in our database name Estee Lauder Inc as the manufacturing or recalling firm.

What the numbers show

Total
3
Critical
0
Severe
0
Most recent
2019-04-24

Of the 3 recalls from Estee Lauder Inc we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) are Severe.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

1–3 of 3

  • LowFDA (Drugs)·D-1132-2019·2019-04-24

    Estee Lauder Recalls Repairwear Cream Due to Ineffective Container Seal

    Estee Lauder Inc is recalling 14,490 jars of Repairwear Laser Focus Line Smoothing Cream SPF 15 because the seal between the cap and jar is ineffective.

    Product
    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
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1452-2014·2014-07-30

    Estee Lauder Recalls DENBLAN Toothpaste Due to Stability Data Issues

    Estee Lauder Inc is recalling 3,791 tubes of DENBLAN Anticavity Fluoride Toothpaste because stability data does not support the product's expiry date.

    Product
    DENBLAN Anticavity Fluoride Toothpaste, Whitening formula, sodium monofluorophosphate 0.76%, 2.6 oz/75 mL tube, Laboratories Darphin, Dist, Paris France
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-151-2013·2013-02-13

    Estee Lauder DayWear Moisturizer Recalled for Potential Sunscreen Instability

    Estee Lauder is recalling DayWear Sheer Tint Release moisturizer because the sunscreen ingredient may be unstable, potentially reducing its effectiveness.

    Product
    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 YO
    Category
    Consumer Product
    Distribution
    Distributed nationwide

About this company

Community-sourced company facts from Wikidata, not from any recall agency. This is background on the corporate entity — it says nothing about the recall(s) listed on this page, which come from the agency source notice above.

Estée Lauder Companies

American-based cosmetics company

Country
United States
Founded
1946

Official website

Source: Wikidata (Q1260606), licensed CC0. Wikidata is community-edited and may not reflect the current corporate structure.