FDA Drug Recalls

Recalls / Class II

Class IID-0217-2018

Product

Shiseido Future Solution LX Luxurious Eye & Lip Collection contains SPF 50+ (octinoxate 4.9%, octocrylebe 3.0%, oxybenzone 1.0% and zinc oxide 15.4%), packaged in 15 mL tubes, Shiseido Americas Corporation Dist. New York, NY 10022

Affected lot / code info
SKU#: 95393

Why it was recalled

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

Recalling firm

Firm
SHISEIDO AMERICA INC.
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
366 Princeton Hightstown Rd, N/A, East Windsor, New Jersey 08520-1411

Distribution

Quantity
N/A
Distribution pattern
Product was distributed nationwide.

Timeline

Recall initiated
2017-12-14
FDA classified
2018-01-12
Posted by FDA
2018-01-24
Terminated
2021-06-24
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0217-2018. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.