Repairwear Laser Focus Line Smoothing Cream Broad Spectrum SPF 15 — Class III drug recall D-1132-2019
Terminated recall by Estee Lauder Inc, reported 2019-04-24, distributed nationwide. Defective container: Ineffective seal between the cap and jar of the affected product.
| Recall number | D-1132-2019 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Estee Lauder Inc, New York, NY, United States |
| Recall initiated | 2019-03-15 |
| Classified | 2019-04-15 |
| Reported by FDA | 2019-04-24 |
| Terminated | 2025-01-13 |
| Distributed | Nationwide (US) |
| Quantity | 14,490 jars |
| Reason classes | packaging |
| Lot numbers | A68 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1132-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.