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.
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