Reported Jan 24, 2018 · Terminated

Shiseido Future Solution LX Universal Defense SPF 50+ (octinoxate 4.9%, octocrylebe 3.0%, oxybenzone 1.0% and zinc…

Shiseido America Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: SHISEIDO AMERICA INC. · 366 Princeton Hightstown Rd · East Windsor, NJ · 08520-1411

Is this the product you have?

3 of 3 products

Products covered by this recall
#Product as published
12mL
215 mL and
350 mL tubes, Shiseido Americas Corporation Dist. New York, NY 10022. NDC 58411-256-60
Lot codes and dates
    • SKU#: a) 8C52541
    • b) 8B41841
    • c) 1155840
    • 1155841
    • 1155842
    • 1155851
    • 0710341
    • 0710342
Amount recalled
N/A

This recall covers 5 products

The agency filed one notice per product. You are reading one of them; the other 4 are below.

Where it was sold

  • Nationwide

Why it was recalled

GMP Deviations: manufacturing of API material did not meet GMP and quality requirements.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA drug enforcement) notice

Notice updated Jun 24, 2021 · Data as of Sep 19, 5:55 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.