# FDA recall D-1132-2019

> **Estee Lauder Inc** · Class III · drug recall initiated 2019-03-15.

## 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

## Reason for recall

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

## Distribution

U.S.A. Nationwide

## Key facts

- **Recall number:** D-1132-2019
- **Recalling firm:** Estee Lauder Inc
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2019-03-15
- **Report date:** 2019-04-24
- **Termination date:** 2025-01-13

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** New York, NY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1132-2019

## Citation

> AI Analytics. FDA recall D-1132-2019. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/D-1132-2019. Source: US FDA. Licensed CC0.

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