Allergan PLC Skin Medica Acne System, Contains: Purifying Foaming Wash recall — FDA D-1410-2020
SUBPOTENT DRUG: Products failed assay results at the 12 and 24 month timepoints.
Overview of recall records associated with Allergan PLC, including dates, categories and classifications where available.
Classification mix: Class III: 1.
SUBPOTENT DRUG: Products failed assay results at the 12 and 24 month timepoints.
This page summarizes recall records in which the official source identifies Allergan PLC 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.