FDA recall record

Vi-Jon Magnesium Citrate Oral Solution recall — FDA D-1054-2017

Microbial contamination of non-sterile products: product was found to contain mold, identified as Rhinocladiella similis.

Class IIclassification
D-1054-2017official record ID
Aug 9, 2017report date

Recall record at a glance

Official recordD-1054-2017
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmVi-Jon, Inc.
Report dateAug 9, 2017
Recall initiation dateJul 17, 2017
Quantity101,244 bottles
LocationSmyrna, TN, United States

Official product description

Magnesium Citrate Oral Solution, packaged in a 10 fl. oz. (296 mL) glass bottle, OTC, labeled as: a) GoodSense Magnesium Citrate Oral Solution Saline Laxative Very Low Sodium, UPC# 846036007381, NDC 50804-686-38, Distributed by: Geiss, Desitin &Dunn, Inc., Peachtree City, GA 30269; b) Premier Value Magnesium Citrate Oral Solution saline laxative very low sodium, UPC# 840986010255, NDC 68016-826-38, Distributed by: Chain Drug Consortium, Boca Raton, FL 33431; c) Swan Very Low Sodium Citroma Magnesium Citrate, UPC# 308690686383, NDC 0869-686-38, Distributed by: Vi-Jon, Smyrna, TN, 37167 ; d) ShopRite Magnesium Citrate Oral Solution Saline Laxative Low Sodium, UPC# 041190211487, NDC 41190-686-38, Distributed by: Wakefern Food Corporation, Jamesburg, NJ 08831

Why the product was recalled

Microbial contamination of non-sterile products: product was found to contain mold, identified as Rhinocladiella similis.

Distribution information

GA, PA, NJ

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

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About this record

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