Estee Lauder Repairwear Laser Focus Line Smoothing Cream Recall

Why it was recalled

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

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

Lot numbers, UPCs & expiration codes

Lot #: A68

Where it was sold

U.S.A. Nationwide

What to do if you have this product

Compare the lot number and expiration date on your package with the codes above.
Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
If you have symptoms you think are related, contact your doctor. In an emergency call 911.
Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number: D-1132-2019
Classification: Class III
Status: Terminated
Recall initiated: Mar 15, 2019
FDA report date: Apr 24, 2019
Quantity: 14490 jars
Recall type: Voluntary: Firm initiated
Recalling firm: Estee Lauder Inc

Original FDA data

Every field from FDA enforcement report D-1132-2019, exactly as published.

Show all FDA fields

City: New York
State: NY
Status: Terminated
Country: United States
Event ID: 82452
Address: 767 5th Ave Fl 47th
Code information: Lot #: A68
Postal code: 10153-0023
Report date: Apr 24, 2019
Product type: Drugs
Recall number: D-1132-2019
Classification: Class III
Recalling firm: Estee Lauder Inc
Product quantity: 14490 jars
Termination date: Jan 13, 2025
Reason for recall: Defective container: Ineffective seal between the cap and jar of the affected product.
Voluntary / mandated: Voluntary: Firm initiated
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
Distribution pattern: U.S.A. Nationwide
Recall initiation date: Mar 15, 2019
Initial firm notification: Letter
Center classification date: Apr 15, 2019

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1132-2019, published Apr 24, 2019. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: Oct 2, 2026. Content last changed: Oct 2, 2026.

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