Vi-Jon Recalls Magnesium Citrate Oral Solution for Impurity Failures
Vi-Jon, Inc. is recalling 87,972 bottles of Magnesium Citrate Oral Solution because the product failed impurities and degradation specifications.
What this means for you
Cosmetic or documentation issue. No expected health impact, but the manufacturer is correcting the affected products.
Our severity reasoning: The agency classified this as an FDA Class III recall, which is defined as unlikely to cause adverse health consequences, aligning with the 'Low' severity criterion for documentation or minor specification issues.
Plain-English summary
Vi-Jon, Inc. is voluntarily recalling 87,972 bottles of Magnesium Citrate Oral Solution Cherry Flavor, 1.745 g per fl oz, packaged in 10 fl. oz (296 mL) bottles. The recall is due to the product failing impurities and degradation specifications.
The affected product is distributed in the United States and Canada under several labels, including CVS Health, Meijer, and Life Brand. The specific lot number is 0323439 with an expiration date of 07/2018.
Consumers should stop using the recalled product and return it to the place of purchase for a refund or contact the recalling firm for further instructions.
The recalled product
- Product
- Magnesium Citrate Oral Solution Cherry Flavor, 1.745 g per fl oz, packaged in 10 fl. oz ( 296 mL) bottles, Labeled as a) CVS Health, Distributed by: CVS Pharmacy, Inc. One CVS Drive, Woonsocket, RI 02895; NDC 6984238038, UPC 050428418321, b) Meijer, Dist. By Meijer Distribution,
- Manufacturer
- Vi-Jon, Inc.
- Category
- Drug — Oral Solution
- Hazard
- Affected units
- 87,972
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Lot #: 0323439 Exp. 07/2018
Distribution
Distribution scope not specified by the agency.
Part of a larger recall action
This product is one of 2 recalled by Vi-Jon, Inc. under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 2 products in this recall →Related recalls
Same manufacturer · Vi-Jon, Inc.
See all →- ModerateHEB Isopropyl Alcohol First Aid Antiseptic Label Mix-Up Recall
FDA (Drugs) · 2022-03-09
- ModerateKroger 70% Isopropyl Alcohol Bottles Mislabeled; Contains Hydrogen Peroxide
FDA (Drugs) · 2021-09-22
- SevereVi-Jon Hydrogen Peroxide Recalled for IPA Contamination
FDA (Drugs) · 2019-03-13
- LowVi-Jon Recalls Equate and Studio 35 Face Moisturizers for Stability Failures
FDA (Drugs) · 2017-11-01
- ModerateVi-Jon Recalls Magnesium Citrate Oral Solution for Impurity Failures
FDA (Drugs) · 2017-10-11
Same hazard · impurities
See all →- LowDabigatran Etexilate Capsules Recalled Due to Impurity Specification Failure
FDA (Drugs) · 2026-08-05
- ModerateGlycopyrrolate Oral Solution Recalled Due to Failed Impurities and Degradation Specifications
FDA (Drugs) · 2026-07-29
- ModerateMethohexital Sodium for Injection Recalled for Failed Impurities and Degradation Specifications
FDA (Drugs) · 2026-07-15
- ModerateMethohexital Sodium 100 mg/10 mL Compounded Drug Recalled Nationwide
FDA (Drugs) · 2026-07-15
- LowFexofenadine Hydrochloride Tablets 180 mg Recalled for Impurities
FDA (Drugs) · 2026-07-08