Vi-Jon, LLC: Drug Recall

Recall #D-0970-2022 · 05/05/2022

Class II: Risk

Recall Details

Recall Number
D-0970-2022
Classification
Class II
Product Type
Drug
Recalling Firm
Vi-Jon, LLC
Status
Terminated
Date Initiated
05/05/2022
Location
Smyrna, TN, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
75,064 bottles

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.

Product Description

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

Distribution Pattern

Nationwide in the USA

Other Recalls by Vi-Jon, LLC

View all recalls by Vi-Jon, LLC →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.