CLASS I Drug recall · Reported 13 Jul 2022 · FDA Enforcement Report

Cvs Health Magnesium Citrate Saline Laxative, Oral Solution recalled

Vi-Jon is recalling Cvs Health Magnesium Citrate Saline Laxative, Oral Solution, Lemon Flavor, distributed nationwide in the US. The recall was initiated on 13 Jun 2022 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot: 0556808 Exp. 12/2023
Quantity recalled98,958 bottles

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-1175-2022
FDA event ID
90443
Recalling firm
Vi-Jon, Smyrna, TN
Classification
Class I
Status
Terminated
Recall initiated
13 Jun 2022
FDA classified
5 Jul 2022
Reported
13 Jul 2022
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Sterility

Timeline

13 Jun 2022Recall initiated by company
5 Jul 2022Classified by FDA+22 days
13 Jul 2022Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Microbial Contamination of a Non-Sterile Products: Testing of product onfirmed the presence of Gluconacetobacter Liquefaciens

A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.

Product as listed by the FDA

CVS Health Magnesium Citrate SALINE LAXATIVE, Oral Solution, 1.745 g, Lemon Flavor, 10 FL OZ (296 mL), Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895, UPC 0 50428 30594 2.

Where it was distributed

Distributed Nationwide in the USA

Nationwide

Stores named: CVS

Questions about this recall

Why was it recalled?

Microbial Contamination of a Non-Sterile Products: Testing of product onfirmed the presence of Gluconacetobacter Liquefaciens

Which lots are affected?

Lot: 0556808 Exp. 12/2023

Where was it sold?

Distributed Nationwide in the USA

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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