FDAFDA · Food and drugs·Recall number D-0944-2017
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.
Published July 12, 2017 · Recall initiated: June 28, 2017
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Presence of Foreign Substance: possibility of the presence of metal in the product.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- PARODONTAX
- Manufacturer
- GSK Consumer Healthcare
- Distributor
- Nationwide in the USA
- Lot
- G7E101, Exp 04/19
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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