Crest 3D White Fluoride Anticavity Toothpaste — Class III drug recall D-1290-2022
Completed recall by The Procter & Gamble Company, reported 2022-08-03, distributed in WA. Labeling: Missing label: the product tube was missing a label and contained a different formulation.
| Recall number | D-1290-2022 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Completed |
| Voluntary or mandated | Voluntary |
| Recalling firm | The Procter & Gamble Company, Cincinnati, OH, United States |
| Recall initiated | 2022-07-08 |
| Classified | 2022-07-26 |
| Reported by FDA | 2022-08-03 |
| Distributed | WA |
| Quantity | 1,128 tubes |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00037000171867 |
| Expiration dates | 2023-10-31 |
Product
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1290-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.