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Stop using now Drug recall · FDA · Published July 18, 2013

Vi-Jon Mouth Rinse Recall: Microbial Contamination Risk

Vi-Jon recalls alcohol-free antiseptic mouth rinse due to Burkholderia contaminans contamination. Check your lot number and expiration date.

🇺🇸 FDA recall #D-812-2013DrugVi-Jon ›
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Recalling firmVi-Jon, Inc.1 Swan Dr. · Smyrna, TN 37167-2099
✎ GovInfoNow plain-language explainer

What happened, in plain English

Vi-Jon, Inc. is recalling Alcohol Free Antiseptic Mouth Rinse because stability samples were found to be contaminated with Burkholderia contaminans. The product was distributed nationwide by The Kroger Co. No remedy or return instructions are currently listed in the record. Read more at govinfonow.com/recall/46842-vi-jon-inc-recalls-alcohol-free-antiseptic-cetylpyridinium-chloride-mouth.

Source Summary by GovInfoNow · govinfonow.com/recall/46842-vi-jon-inc-recalls-alcohol-free-antiseptic-cetylpyridinium-chloride-mouth · Updated October 13, 2026 · FDA enforcement record: FDA #D-812-2013

Cite this page

“Vi-Jon Mouth Rinse Recall: Microbial Contamination Risk.” GovInfoNow, updated October 13, 2026. https://govinfonow.com/recall/46842-vi-jon-inc-recalls-alcohol-free-antiseptic-cetylpyridinium-chloride-mouth. Based on FDA recall #D-812-2013 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-812-2013%22&limit=1).

Why it’s dangerous

The mouth rinse is contaminated with Burkholderia contaminans, a bacterium that can cause infections, particularly in individuals with weakened immune systems or open wounds in the mouth.

Who’s affected

Consumers who purchased Vi-Jon Alcohol Free Antiseptic Mouth Rinse from Kroger stores nationwide between distribution and July 18, 2013. Individuals with compromised immune systems may be at higher risk from the bacterial contamination.

How to tell if you have this one

Look for Vi-Jon brand Alcohol Free Antiseptic Mouth Rinse, 0.07% mint flavor, in a 33.8 FL OZ (1 L) bottle. Check for UPC 0 41260 33606 5 and Lot # 0185828 with an expiration date of 12/14.

  • Brand
    Vi-Jon
  • Product
    ALCOHOL FREE ANTISEPTIC (cetylpyridinium chloride) Mouth Rinse, 0.07%, mint, 33.8 FL OZ (1 L) bottle, Distributed By
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Stop using the product

    Do not use the mouth rinse if it matches the recalled lot number and expiration date.

  2. Check your bottle details

    Verify that you have Lot # 0185828 and an expiration date of 12/14 on the 33.8 FL OZ bottle.

  3. Contact Kroger for assistance

    Since no remedy is listed, contact The Kroger Co. in Cincinnati, OH, to inquire about returns or refunds.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA terminated this recall 11 months after the firm started it.

1. Firm started the recall: Jul 18, 201312. FDA classified it Class III: Jul 22, 201323. Published in FDA’s Enforcement Report: Jul 31, 201334. FDA terminated the recall: Jun 17, 2014420132014
  1. Firm started the recall
  2. FDA classified it Class III
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #D-812-2013 (July 18, 2013) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-812-2013 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 13, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA