DrugJan 24, 2018
Shiseido Future Solution LX Universal Defense SPF 50+ recall — FDA D-0215-2018
GMP Deviations: manufacturing of API material did not meet GMP and quality requirements.
Class IIFDA: TerminatedSHISEIDO AMERICA Inc.
Recall history in this database
Classification mix: Class II: 5.
DrugJan 24, 2018
Shiseido Future Solution LX Discovery Set contains SPF 50+ recall — FDA D-0216-2018
GMP Deviations: manufacturing of API material did not meet GMP and quality requirements.
Class IIFDA: TerminatedSHISEIDO AMERICA Inc.
DrugJan 24, 2018
SHISEIDO bareMinerals Broad Spectrum SPF 50 Daily Prep Lotion recall — FDA D-0214-2018
GMP Deviations: manufacturing of API material did not meet GMP and quality requirements.
Class IIFDA: TerminatedSHISEIDO AMERICA Inc.
DrugJan 24, 2018
Shiseido Future Solution LX Luxurious Eye & Lip Collection contains SPF 50+ recall — FDA D-0217-2018
GMP Deviations: manufacturing of API material did not meet GMP and quality requirements.
Class IIFDA: TerminatedSHISEIDO AMERICA Inc.
DrugJan 24, 2018
Shiseido Future Solutions LX Triple Points Bonus contains SPF 50+ recall — FDA D-0218-2018
GMP Deviations: manufacturing of API material did not meet GMP and quality requirements.
Class IIFDA: TerminatedSHISEIDO AMERICA Inc.
Understanding this recall history
This page summarizes recall records in which the official source identifies SHISEIDO AMERICA Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.