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Stop using now Drug recall · FDA · Published July 17, 2017

Vi-Jon Magnesium Citrate Oral Solution Recall: Microbial Contamination Risk

Vi-Jon recalls Magnesium Citrate Oral Solution with mold contamination. Product contains Rhinocladiella similis mold. Consumers should stop using affected lots.

🇺🇸 FDA recall #D-1054-2017DrugVi-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 has recalled Magnesium Citrate Oral Solution in 10 fl. oz. glass bottles due to mold contamination. Using this product could cause illness from the mold. People should stop using the recalled items immediately. Read more at govinfonow.com/recall/41435-vi-jon-magnesium-citrate-oral-solution-recall-microbial-contamination-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/41435-vi-jon-magnesium-citrate-oral-solution-recall-microbial-contamination-risk · Updated October 7, 2026 · FDA enforcement record: FDA #D-1054-2017

Cite this page

“Vi-Jon Magnesium Citrate Oral Solution Recall: Microbial Contamination Risk.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/41435-vi-jon-magnesium-citrate-oral-solution-recall-microbial-contamination-risk. Based on FDA recall #D-1054-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1054-2017%22&limit=1).

Why it’s dangerous

The product contains mold identified as Rhinocladiella similis. This mold can cause illness, especially in people with weakened immune systems. Using the product may lead to infections or other health issues.

Who’s affected

People who own or use the recalled Magnesium Citrate Oral Solution in 10 fl. oz. glass bottles labeled as GoodSense or similar brands. Those with compromised immune systems are at higher risk of illness.

How to tell if you have this one

Check for the product labeled as GoodSense Magnesium Citrate Oral Solution Saline Laxative Very Low Sodium. Look for the UPC# 846036007381 or NDC 50804-686-38. Also check for lot numbers 0341906 or 0343709 with expiration dates up to December 2018 or January 2019.

  • Brand
    Vi-Jon
  • Product
    Magnesium Citrate Oral Solution, packaged in a 10 fl. oz. (296 mL) glass bottle, OTC, labeled as: a) GoodSense
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Stop Using It Now

    Immediately stop using the recalled Magnesium Citrate Oral Solution if you have the affected product.

Where it went and when

Where it was distributed

Distributed in 3 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: yesPANew Jersey: yesNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: yesGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

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

States: Georgia, New Jersey, Pennsylvania.

Recall timeline

FDA terminated this recall 2.5 years after the firm started it.

1. Firm started the recall: Jul 17, 201712. FDA classified it Class II: Aug 3, 201723. Published in FDA’s Enforcement Report: Aug 9, 201734. FDA terminated the recall: Jan 24, 2020420172020
  1. Firm started the recall
  2. FDA classified it Class II
  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-1054-2017 (July 17, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1054-2017 to see it in context.
  • Plain-language summary written by qwen3:4b on October 7, 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