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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 82452

1 recalled-product record grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
March 15, 2019
Product types
Drug
Classifications
Class III
Statuses
Terminated
Recalling firm wording
Estee Lauder Inc

Dossier provenance

Source snapshots represented here

  • openFDA Drug Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

drug · product 1 of 1

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

D-1132-2019
Recall number
D-1132-2019
Initiated
March 15, 2019
Classification
Class III
Status
Terminated
Recalling firm
Estee Lauder Inc
Quantity
14490 jars

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Defective container: Ineffective seal between the cap and jar of the affected product.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

Lot #: A68

Distribution pattern

U.S.A. Nationwide