Severity
Low
LowClass IIITerminated
FDA Drug recall · Reported February 13, 2013
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
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.
Estee Lauder Inc recalled ESTEE LAUDER DayWear Sheer Tint Release, Advanced Multi-Protection Anti-Oxidant Moisturi… - a low-severity action.
ESTEE LAUDER DayWear Sheer Tint Release, Advanced Multi-Protection Anti-Oxidant Moisturi… was recalled by Estee Lauder Inc in February 13, 2013. Reason: Failed Stability Specifications: The active sunscreen ingredient, avobenzone 3%, may not be stable over the s…. Check the official notice for the remedy. Verify recall #D-151-2013 with the FDA Drug before acting.
The recall
Estee Lauder Inc issued this low-severity FDA Drug recall-Failed Stability Specifications: The active sunscreen ingredient, avobenzone 3%, may not be stable over the s….
- Low
- severity level
- Class III
- classification
- February 13, 2013
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-151-2013 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-151-2013) was formally reported on February 13, 2013, with the manufacturer initiating the action on October 23, 2012. It is classified under Low severity (Class III), with a current status of Terminated. Estee Lauder Inc is listed as the recalling firm, operating out of New York, NY. Federal records list the affected scope as 1.7 oz. 241,236 tubes; 1.5 mL sample size 544,548 foil packs.
The documented reason for this recall is: 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. Distribution data in the federal record shows the product reached: Nationwide, Puerto Rico, Bermuda and Panama. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Household Products recalls over time
Where this recall sits in its category - 3,056 household products recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified low severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
1.7 oz. 241,236 tubes; 1.5 mL sample size 544,548 foil packs
Related Recalls
6
0 from same agency
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.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | D-151-2013 |
| Date reported | February 13, 2013 |
| Date initiated | October 23, 2012 |
| Recalling firm | Estee Lauder Inc |
| Firm location | New York, NY |
| Affected scope | 1.7 oz. 241,236 tubes; 1.5 mL sample size 544,548 foil packs |
| Distribution | Nationwide, Puerto Rico, Bermuda and Panama |
Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (D-151-2013) and product description against the item you own. Search the archive
- Confirm the current status with FDA Drug before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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.
Where was the recalled product distributed? ▼
Distribution: Nationwide, Puerto Rico, Bermuda and Panama.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-151-2013) against your product. Visit the official FDA Drug website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Drug, reported February 13, 2013. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.