Vi-Jon recalls 32 fl oz hydrogen peroxide antiseptic solution due to cross contamination with isopropyl alcohol. This may cause unintended effects when used for first aid. No remedy specified in official notice.
“Vi-Jon Hydrogen Peroxide Antiseptic Solution Recall: Cross Contamination Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/39185-vi-jon-hydrogen-peroxide-antiseptic-solution-recall-cross-contamination-risk. Based on FDA recall #D-0520-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0520-2019%22&limit=1).
The FDA announced on Feb. 20, 2019, that Vi-Jon, Inc. voluntarily recalled Topical Solution USP Hydrogen Peroxide First Aid Antiseptic Oral Debriding Agent due to cross contamination with isopropyl alcohol (IPA).
How to tell if you have it
Brand: Vi-Jon
Product: Topical Solution USP Hydrogen Peroxide First Aid Antiseptic Oral Debriding Agent 32 Fl. Oz. (1 QT) 946 mL bottle
UPC: 0-93351-12758-8
Lot: 0384244
Expiration: 01/2020
Distributed By: Discount Drug Mart, Medina, Ohio
Distribution area: Ohio
Units affected: 6756 bottles
The hazard
The recall addresses the presence of IPA in the finished product. The FDA classified this as a Class II recall.
Context
GovInfoNow's records show Vi-Jon, Inc. has 7 other recalls on record since July 18, 2013. Other recent recalls of similar products include Cardinal Health 200 Webcol Alcohol Prep Pads Recall (March 2, 2026), Zep Alcohol Sanitizer Spray Recall (May 22, 2026), and Sage Products 2% Chlorhexidine Cloth Recall (Aug. 18, 2026).
How to tell if you have this one
Look for the 32 fl oz (946 mL) bottle labeled 'Topical Solution USP Hydrogen Peroxide First Aid Antiseptic Oral Debriding Agent'. It was distributed by Discount Drug Mart with NDC 53943-871-45 and lot number 0384244.
Brand
Vi-Jon
Product
Topical Solution USP Hydrogen Peroxide First Aid Antiseptic Oral Debriding Agent 32 Fl. Oz. (1 QT) 946 mL bottle
Category
Drug
Based on the official FDA remedy
What to do — step by step
Check Product Details
Identify if your product matches the description: 32 fl oz (946 mL) bottle with NDC 53943-871-45 and lot 0384244.
Where it went and when
Where it was distributed
Distributed in Ohio.
Listed by the agency
Not listed
FDA distribution: “Distributed in Ohio” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Ohio.
Recall timeline
FDA terminated this recall 15 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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-0520-2019 (February 20, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0520-2019 to see it in context.
Plain-language summary written by qwen3:4b on October 5, 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.