parodontax WHITENING — Class II drug recall D-0944-2017
Terminated recall by GSK Consumer Healthcare, reported 2017-07-12, distributed nationwide. Presence of Foreign Substance: possibility of the presence of metal in the product.
| Recall number | D-0944-2017 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | GSK Consumer Healthcare, Warren, NJ, United States |
| Recall initiated | 2017-06-28 |
| Classified | 2017-07-06 |
| Reported by FDA | 2017-07-12 |
| Terminated | 2020-02-07 |
| Distributed | Nationwide (US) |
| Quantity | 15,708 tubes |
| NDC | 00135-0598, 00135-0598-01, 00135-0598-02, 00135-0599, 00135-0599-01, 00135-0599-02, 00135-0601, 00135-0601-01, 00135-0601-02 |
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 for recall
Presence of Foreign Substance: possibility of the presence of metal in the product.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0944-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.