parodontax WHITENING (Stannous fluoride) Daily Fluoride Anticavity and Antigingivitis recall — FDA D-0944-2017
Presence of Foreign Substance: possibility of the presence of metal in the product.
Overview of recall records associated with GSK Consumer Healthcare, including dates, categories and classifications where available.
Classification mix: Class II: 2, Class III: 1.
Presence of Foreign Substance: possibility of the presence of metal in the product.
Presence of Foreign Substance; low concentration of an additional flavoring ingredient, Patchouli oil resulting in complaints of off flavor/scent
Labeling Not Elsewhere Classified: front labels have the incorrect NDC or 0145-1506-01 instead of the correct NDC of 0145-1506-05 and some back labels have the incorrect indication stating…
This page summarizes recall records in which the official source identifies GSK Consumer Healthcare 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.