US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jun 28, 2017 (9 years ago)

parodontax WHITENING (Stannous fluoride) Daily Fluoride Anticavity and Antigingivitis…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Presence of Foreign Substance: possibility of the presence of metal in the product.

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.

Recalling firm
GSK Consumer Healthcare
NDC code
0135-0601-01
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0944-2017

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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