PlainRecalls
FDA Drug Moderate Class II Terminated

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.