3M ESPE Clinpro 5000 — Class III drug recall D-0376-2015
Terminated recall by 3M Company/3m Espe Dental Products, reported 2015-01-28, distributed nationwide. Labeling: Incorrect or Missing Lot and/or Exp. Date - The subject lot is missing the lot number and expiration
| Recall number | D-0376-2015 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | 3M Company/3m Espe Dental Products, Saint Paul, MN, United States |
| Recall initiated | 2014-12-19 |
| Classified | 2015-01-20 |
| Reported by FDA | 2015-01-28 |
| Terminated | 2015-04-14 |
| Distributed | Nationwide (US) |
| Quantity | 19,728 tubes |
| Reason classes | labeling |
| NDC | 48878-3130-04 |
| Lot numbers | 30131 |
Product
3M ESPE Clinpro 5000 (1.1% Sodium Flouride), Anti-Cavity Toothpaste, 4 oz tube (NDC 48878-3130-04), Rx Only, Manufactured for 3M ESPE Dental Products, St. Paul, MN 55144
Reason for recall
Labeling: Incorrect or Missing Lot and/or Exp. Date - The subject lot is missing the lot number and expiration date stamp on the primary box..
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-0376-2015. 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.