ESTEE LAUDER DayWear Sheer Tint Release recall
ESTEE LAUDER DayWear Sheer Tint Release, Advanced Multi-Protection Anti-Oxidant Moisturizer Broad Spectrum SPF15, All Skin types, 1.7 FL. OZ. LIQ/50…
Why was ESTEE LAUDER DayWear Sheer Tint Release 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.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
A70, A80, AA0, B11, A31, A51, B51, A81, A91, A12, A22, A72, BA0, AB0, BB0, CB0, AC0, BC0, A11, A21, B21, B31, A41.
- Product
- ESTEE LAUDER DayWear Sheer Tint Release, Advanced Multi-Protection Anti-Oxidant Moisturizer Broad Spectrum SPF15, All Skin types, 1.7 FL. OZ. LIQ/50…
- Recalling firm
- Estee Lauder Inc
- Quantity
- 1.7 oz. 241,236 tubes; 1.5 mL sample size 544,548 foil packs
- Distribution
- Nationwide, Puerto Rico, Bermuda and Panama
- Recall date
- February 13, 2013
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)