PlainRecalls
FDA Drug Low Class III Terminated

ESTEE LAUDER DayWear Sheer Tint Release, Advanced Multi-Protection Anti-Oxidant Moisturizer Broad Spectrum SPF15, All Skin types, 1.7 FL. OZ. LIQ/50 ml (tube inside a unit carton) with UPC No. 2713179904, Code WKEM-01, and 1.5 mL foil sample packets, ESTEE LAUDER, DIST., NEW YORK, N.Y. 10022 NDC 11559-008-01

Reported: February 13, 2013 Initiated: October 23, 2012 #D-151-2013

Product Description

ESTEE LAUDER DayWear Sheer Tint Release, Advanced Multi-Protection Anti-Oxidant Moisturizer Broad Spectrum SPF15, All Skin types, 1.7 FL. OZ. LIQ/50 ml (tube inside a unit carton) with UPC No. 2713179904, Code WKEM-01, and 1.5 mL foil sample packets, ESTEE LAUDER, DIST., NEW YORK, N.Y. 10022 NDC 11559-008-01

Reason for Recall

Failed Stability Specifications: The active sunscreen ingredient, avobenzone 3%, may not be stable over the shelf life, the sunscreen effectiveness may be less than labeled.

Details

Recalling Firm
Estee Lauder Inc
Units Affected
1.7 oz. 241,236 tubes; 1.5 mL sample size 544,548 foil packs
Distribution
Nationwide, Puerto Rico, Bermuda and Panama
Location
New York, NY

Frequently Asked Questions

What product was recalled?
ESTEE LAUDER DayWear Sheer Tint Release, Advanced Multi-Protection Anti-Oxidant Moisturizer Broad Spectrum SPF15, All Skin types, 1.7 FL. OZ. LIQ/50 ml (tube inside a unit carton) with UPC No. 2713179904, Code WKEM-01, and 1.5 mL foil sample packets, ESTEE LAUDER, DIST., NEW YORK, N.Y. 10022 NDC 11559-008-01. Recalled by Estee Lauder Inc. Units affected: 1.7 oz. 241,236 tubes; 1.5 mL sample size 544,548 foil packs.
Why was this product recalled?
Failed Stability Specifications: The active sunscreen ingredient, avobenzone 3%, may not be stable over the shelf life, the sunscreen effectiveness may be less than labeled.
Which agency issued this recall?
This recall was issued by the FDA Drug on February 13, 2013. Severity: Low. Recall number: D-151-2013.