Severity
Low
LowClass IIICompleted
FDA Drug recall · Reported August 3, 2022
Crest 3D White Fluoride Anticavity Toothpaste, Advanced Triple Whitening, 0.243% sodium fluoride, Net Wt. 5.6 oz (158 g) a) Individual carton, UPC 0 37000 598534; b) 5-count Bundle, UPC 037000171867, Distributed. By Procter & Gamble, Cincinnati, OH 45202.
Labeling: Missing label: the product tube was missing a label and contained a different formulation.
The Procter & Gamble Company recalled Crest 3D White Fluoride Anticavity Toothpaste, Advanced Triple Whitening, 0.243% sodium f… - a low-severity action.
Crest 3D White Fluoride Anticavity Toothpaste, Advanced Triple Whitening, 0.243% sodium f… was recalled by The Procter & Gamble Company in August 3, 2022. Reason: Labeling: Missing label: the product tube was missing a label and contained a different formulation.. Check the official notice for the remedy. Verify recall #D-1290-2022 with the FDA Drug before acting.
The recall
The Procter & Gamble Company issued this low-severity FDA Drug recall-Labeling: Missing label: the product tube was missing a label and contained a different formulation..
- Low
- severity level
- Class III
- classification
- August 3, 2022
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-1290-2022 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-1290-2022) was formally reported on August 3, 2022, with the manufacturer initiating the action on July 8, 2022. It is classified under Low severity (Class III), with a current status of Completed. The Procter & Gamble Company is listed as the recalling firm, operating out of Cincinnati, OH. Federal records list the affected scope as 1,128 tubes.
The documented reason for this recall is: Labeling: Missing label: the product tube was missing a label and contained a different formulation. Distribution data in the federal record shows the product reached: Washington State. 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 low severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
1,128 tubes
Related Recalls
6
3 from same agency
Product description
Crest 3D White Fluoride Anticavity Toothpaste, Advanced Triple Whitening, 0.243% sodium fluoride, Net Wt. 5.6 oz (158 g) a) Individual carton, UPC 0 37000 598534; b) 5-count Bundle, UPC 037000171867, Distributed. By Procter & Gamble, Cincinnati, OH 45202.
Reason for recall
Labeling: Missing label: the product tube was missing a label and contained a different formulation.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Completed |
| Recall number | D-1290-2022 |
| Date reported | August 3, 2022 |
| Date initiated | July 8, 2022 |
| Recalling firm | The Procter & Gamble Company |
| Firm location | Cincinnati, OH |
| Affected scope | 1,128 tubes |
| Distribution | Washington State |
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-1290-2022) 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? ▼
Crest 3D White Fluoride Anticavity Toothpaste, Advanced Triple Whitening, 0.243% sodium fluoride, Net Wt. 5.6 oz (158 g) a) Individual carton, UPC 0 37000 598534; b) 5-count Bundle, UPC 037000171867, Distributed. By Procter & Gamble, Cincinnati, OH 45202.. Recalled by The Procter & Gamble Company. Units affected: 1,128 tubes.
Why was this product recalled? ▼
Labeling: Missing label: the product tube was missing a label and contained a different formulation.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on August 3, 2022. Severity: Low. Recall number: D-1290-2022.
Where was the recalled product distributed? ▼
Distribution: Washington State.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-1290-2022) 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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Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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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 August 3, 2022. 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.