Severity
Moderate
ModerateClass IITerminated
FDA Drug recall · Reported July 12, 2017
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.
Presence of Foreign Substance: possibility of the presence of metal in the product.
Compiled from official public sources by the editorial team.
Verify with FDA Drug →
Gsk Consumer Healthcare recalled parodontax WHITENING (Stannous fluoride) Daily Fluoride Anticavity and Antigingivitis Too… - a moderate-severity action.
parodontax WHITENING (Stannous fluoride) Daily Fluoride Anticavity and Antigingivitis Too… was recalled by Gsk Consumer Healthcare in July 12, 2017. Reason: Presence of Foreign Substance: possibility of the presence of metal in the product.. Check the official notice for the remedy. Verify recall #D-0944-2017 with the FDA Drug before acting.
The recall
Gsk Consumer Healthcare issued this moderate-severity FDA Drug recall-Presence of Foreign Substance: possibility of the presence of metal in the product..
- Moderate
- severity level
- Class II
- classification
- July 12, 2017
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-0944-2017 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-0944-2017) was formally reported on July 12, 2017, with the manufacturer initiating the action on June 28, 2017. It is classified under Moderate severity (Class II), with a current status of Terminated. Gsk Consumer Healthcare is listed as the recalling firm, operating out of Warren, NJ. Federal records list the affected scope as 15,708 tubes.
The documented reason for this recall is: Presence of Foreign Substance: possibility of the presence of metal in the product. Distribution data in the federal record shows the product reached: Nationwide in the USA. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 3 from FDA Drug - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Cosmetics & Personal Care recalls over time
Where this recall sits in its category - 1,360 cosmetics & personal care recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
15,708 tubes
Related Recalls
6
3 from same agency
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.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | D-0944-2017 |
| Date reported | July 12, 2017 |
| Date initiated | June 28, 2017 |
| Recalling firm | Gsk Consumer Healthcare |
| Firm location | Warren, NJ |
| Affected scope | 15,708 tubes |
| Distribution | Nationwide in the USA |
Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (D-0944-2017) and product description against the item you own. Search the archive
- Confirm the current status with FDA Drug before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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.
Where was the recalled product distributed? ▼
Distribution: Nationwide in the USA.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-0944-2017) against your product. Visit the official FDA Drug website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Drug, reported July 12, 2017. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.