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.
Reported: July 12, 2017 Initiated: June 28, 2017 #D-0944-2017
Product Description
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.
Details
- Recalling Firm
- GSK Consumer Healthcare
- Units Affected
- 15,708 tubes
- Distribution
- Nationwide in the USA
- Location
- Warren, NJ
Frequently Asked Questions
What product 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.. Recalled by GSK Consumer Healthcare. Units affected: 15,708 tubes.
Why was this product recalled? ▼
Presence of Foreign Substance: possibility of the presence of metal in the product.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on July 12, 2017. Severity: Moderate. Recall number: D-0944-2017.
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