May 2022 FDA Recall Drug by Vi-jon, Llc
D-0970-2022 - Superpotent Drug

This Class II drug recall was voluntarily initiated by Vi-jon, Llc on May 5, 2022 for the product Drug. The FDA reported the reason for recall as superpotent drug. The product was distributed Nationwide and the recall is currently terminated.

Recall Number: D-0970-2022

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.
Initiated
05-05-2022
Reported
06-08-2022
Quantity
75,064 bottles

Recall Profile & Regulatory Data

Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Nationwide in the USA
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

Batch or Lot Expiration Information

Lot# Lots: 0559696, 0563041, Exp. 02/2024