FDA Drug recall D-1132-2019
Repairwear Laser Focus Line Smoothing Cream Broad Spectrum SPF 15, packaged in a light green folding carton containing a 50 mL silver jar w…
- FDA Drug
- Class III
- terminated
- Published 2019-04-24
On 2019-04-24 the FDA classified a Class III recall of Repairwear Laser Focus Line Smoothing Cream Broad Spectrum SPF 15, packaged in a light green folding carton containing a 50 mL silver jar w… by Estee Lauder, citing defective container: Ineffective seal between the cap and jar of the affected product.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1132-2019 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2019-03-15 |
| Published | 2019-04-24 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Estee Lauder |
| Distribution | US |
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
Defective container: Ineffective seal between the cap and jar of the affected product.
Identifiers
| code_info | Lot #: A68 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1132-2019%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.