Vi-Jon, LLC: Drug Recall
Recall #D-1173-2023 · 09/05/2023
Class III: Low Risk
Recall Details
- Recall Number
- D-1173-2023
- Classification
- Class III
- Product Type
- Drug
- Recalling Firm
- Vi-Jon, LLC
- Status
- Terminated
- Date Initiated
- 09/05/2023
- Location
- Smyrna, TN, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 245,904 Bottles
Reason for Recall
Incorrect/Undeclared Excipients.
Product Description
Kroger Mint Burst ANTISEPTIC MOUTH RINSE ANTIGINGIVITIS/ANTIPLAQUE (Eucalyptol 0.092%, menthol 0.042%, Methyl salicylate 0.06%, thymol 0.064%), packaged in 16.9 FL OZ (500 mL) bottle, DISTRIBUTED BY THEKROGER CO. CINCINNATI, OHIO 45202, UPC 011110380807
Distribution Pattern
The consignee list includes one distributor with seven distribution centers. No product was sold under government contract. No product was sold to any federal, state, or local agency in the school lunch program.
Other Recalls by Vi-Jon, LLC
- Class I: Dangerous 07/15/2022
- Class I: Dangerous 07/15/2022
- Class I: Dangerous 07/15/2022
- Class II: Risk 07/15/2022
- Class II: Risk 07/15/2022
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.