Vi-Jon, LLC Voluntarily Recalls CVS Magnesium Citrate Saline Laxative Oral Solution Lemon Flavor as It Contains Microbial Contamination

Vi-Jon, LLC Voluntarily Recalls CVS Magnesium Citrate Saline Laxative Oral Solution Lemon Flavor

Smyrna, TN, Vi-Jon, LLC has issued a voluntary nationwide recall of one lot of CVS Magnesium Citrate Saline Laxative Oral Solution Lemon Flavor 10 FL OZ (296 mL) due to the potential that it may be contaminated with bacteria.

The consumer-level recall was initiated after testing revealed the presence of the bacteria Gluconacetobacter liquefaciens.

Risk Statement

Immunocompromised patients who consume this product may suffer invasive infections usually caused by the bacteria Gluconacetobacter liquefaciens. This could lead to sepsis, a potentially life-threatening complication caused by the body’s response to an infection.

In healthy individuals, this product may cause minor gastrointestinal distress, such as bloating, gas, and diarrhea.

This product is used to treat constipation and usually induces bowel movement in 1/2 to 6 hours. The product, which is packed in a 10 oz clear round plastic bottle, is sold over the counter.

You can identify the affected products with their batch number: 0556808 and expiration date: 12/2023, indicated on the shoulder of the bottle.

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The affected product was distributed to CVS stores nationwide. Vi-Jon, LLC has sent notifications to the stores by email and phone and is arranging for the return of the affected products.

Customers who have purchased this product should discontinue use and return it to the store.

Consumers with questions can email Vi-Jon, LLC customer service at [email protected] Monday through Friday, 7:30 am to 4:30 pm Central Time.

Consumers who experience any problems related to this recall should contact their physician.

Any adverse reactions or quality issues experienced with the use of this product should be reported to the FDA’s MedWatch Adverse Event Reporting program at www.FDA.gov/medwatch or by calling 1-800-FDA-1088.

This recall is being conducted in cooperation with the U.S. Food and Drug Administration (FDA).

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