FDA Drug recall D-0944-2017
parodontax WHITENING (Stannous fluoride) Daily Fluoride Anticavity and Antigingivitis Toothpaste, 0.454% (0.15% w/v fluoride ion), 3.4 OZ (…
- FDA Drug
- Class II
- terminated
- Published 2017-07-12
On 2017-07-12 the FDA classified a Class II recall of parodontax WHITENING (Stannous fluoride) Daily Fluoride Anticavity and Antigingivitis Toothpaste, 0.454% (0.15% w/v fluoride ion), 3.4 OZ (… by Gsk Consumer Healthcare, citing presence of Foreign Substance: possibility of the presence of metal in the product.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0944-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-06-28 |
| Published | 2017-07-12 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Gsk Consumer Healthcare |
| Distribution | US |
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.
Reason
Presence of Foreign Substance: possibility of the presence of metal in the product.
Identifiers
| ndc | 0135-0598-01 |
|---|---|
| ndc | 0135-0598-02 |
| ndc | 0135-0599-01 |
| ndc | 0135-0599-02 |
| ndc | 0135-0601-01 |
| ndc | 0135-0601-02 |
| code_info | G7E101, Exp 04/19 |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0944-2017%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.