# FDA recall D-0944-2017

> **GSK Consumer Healthcare** · Class II · drug recall initiated 2017-06-28.

## 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.

## Distribution

Nationwide in the USA

## Key facts

- **Recall number:** D-0944-2017
- **Recalling firm:** GSK Consumer Healthcare
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2017-06-28
- **Report date:** 2017-07-12
- **Termination date:** 2020-02-07

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Warren, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0944-2017

## Citation

> AI Analytics. FDA recall D-0944-2017. Retrieved 2026-06-08 from https://api.ai-analytics.org/recall/D-0944-2017. Source: US FDA. Licensed CC0.

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