GSK Consumer Healthcare recalls parodontax WHITENING (Stannous fluoride) Daily Fluoride Anticavity and Antigingivitis Toothpaste, 0.454% (0.15% w/v flu…
- Recall date
- June 28, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-0944-2017
- FDA classification
- Class II
- Brand / firm
- GSK Consumer Healthcare
- Sold / distributed
- Nationwide in the USA
Why it was recalled
Presence of Foreign Substance: possibility of the presence of metal in the product.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
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.
Get recall alerts
Free email alert whenever GSK Consumer Healthcare has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: GSK Consumer Healthcare