Equate Tartar Control Plus — Class II drug recall D-0970-2022
Terminated recall by Vi-Jon, LLC, reported 2022-06-08, distributed nationwide. Superpotent Drug: product complaint for milky blue appearance and consistency, further investigation by the fi
| Recall number | D-0970-2022 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Vi-Jon, LLC, Smyrna, TN, United States |
| Recall initiated | 2022-05-05 |
| Classified | 2022-05-27 |
| Reported by FDA | 2022-06-08 |
| Terminated | 2024-07-05 |
| Distributed | Nationwide (US) |
| Quantity | 75,064 bottles |
| Reason classes | potency, specification failure |
| UPC / GTIN / UDI-DI | 00681131148009 |
| Lot numbers | 0559696, 0563041 |
| Expiration dates | 2024-02 |
Product
Equate Tartar Control Plus (Eucalyptol 0.092%, Menthol 0.042%, Methyl salicylate 0.060%, Thymol 0.064%) Antiseptic Mouthrise Plus, Antigingivitis/Antiplaque, Blue Mint, 1.5 Liter (50.7 FL OZ) bottle, Distributed By: Wal-Mart Stores, Inc., Bentonville, AR 72716, UPC 6 81131 14800 9
Reason for recall
Superpotent Drug: product complaint for milky blue appearance and consistency, further investigation by the firm found the recalled lots out of specification for the four active ingredients.
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-0970-2022. 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.