D-1132-2019 Class III Terminated
FDA drug recall D-1132-2019 was initiated by Estee Lauder Inc on March 15, 2019 and is designated Class III. Reason for recall: Defective container: Ineffective seal between the cap and jar of the affected product. The recall status is terminated (terminated January 13, 2025). Affected quantity: 14490 jars.
Recall Details
- Product Type
- Drugs
- Report Date
- April 24, 2019
- Initiation Date
- March 15, 2019
- Termination Date
- January 13, 2025
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 14490 jars
Product Description
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 Pattern
U.S.A. Nationwide
Code Information
Lot #: A68