FDA recall record

The Procter & Gamble Company Crest 3D White Fluoride Anticavity Toothpaste, Advanced Triple recall — FDA D-1290-2022

Labeling: Missing label: the product tube was missing a label and contained a different formulation.

Class IIIclassification
D-1290-2022official record ID
Aug 3, 2022report date

Recall record at a glance

Official recordD-1290-2022
CategoryDrug Recalls
ClassificationClass III
FDA record statusCompleted
Recalling firmThe Procter & Gamble Company
Report dateAug 3, 2022
Recall initiation dateJul 8, 2022
Quantity1,128 tubes
LocationCincinnati, OH, United States

Official 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.

Why the product was recalled

Labeling: Missing label: the product tube was missing a label and contained a different formulation.

Distribution information

Washington State

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.