# FDA recall D-0970-2022

> **Vi-Jon, LLC** · Class II · drug recall initiated 2022-05-05.

## 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.

## Distribution

Nationwide in the USA

## Key facts

- **Recall number:** D-0970-2022
- **Recalling firm:** Vi-Jon, LLC
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2022-05-05
- **Report date:** 2022-06-08
- **Termination date:** 2024-07-05

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Smyrna, TN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0970-2022

## Citation

> AI Analytics. FDA recall D-0970-2022. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/D-0970-2022. Source: US FDA. Licensed CC0.

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