GSK Consumer Healthcare recalls parodontax WHITENING (Stannous fluoride) Daily Fluoride Anticavity and Antigingivitis Toothpaste, 0.454% (0.15% w/v fluo
Recalled July 12, 2017 · FDA recall D-0944-2017 · GSK Consumer Healthcare
Hazard
Presence of Foreign Substance: possibility of the presence of metal in the product. · FDA Class II
Units
15,708 tubes
Sold at
Nationwide in the USA
Description
Presence of Foreign Substance: possibility of the presence of metal in the product.
Product
parodontax WHITENING (Stannous fluoride) Daily Fluoride Anticavity and Antigingivitis Toothpaste, 0.454% (0.15% w/v fluoride ion), 3.4 OZ (96.4 g) tube, Distributed by: GSK Consumer Healthcare, Warren, NJ 07059, NDC 0135-0601-01.
Manufacturer(s)
GSK Consumer Healthcare
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →