Home / Recalls / GSK Consumer Healthcare / D-0944-2017

D-0944-2017 Class II Terminated

Recalled by GSK Consumer Healthcare — Warren, NJ

Recall Details

Product Type
Drugs
Report Date
July 12, 2017
Initiation Date
June 28, 2017
Termination Date
February 7, 2020
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
15,708 tubes

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.

Distribution Pattern

Nationwide in the USA

Code Information

G7E101, Exp 04/19

Other recalls by GSK Consumer Healthcare

  • D-0624-2017 Class II — Sensodyne Repair & Protect Whitening, (stannous fluoride 0.45% (0.15% w/v fluori (March 6, 2017)
  • D-0142-2017 Class III — Zeasorb AF (miconazole nitrate), 2%, cures most athlete's foot, Net wt. 2.5 OZ ( (October 18, 2016)
  • Z-2148-2016 Class III — Breathe Right Clear, 30 ct. carton., UPC 7-57145-00246-7 (US), UPC 9-300673-8717 (April 25, 2016)