Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Class II · Moderate risk Ongoing Initiated Dec 21, 2023 (3 years ago)

Freskaro refresh & revitalize Magnesium Citrate Saline Laxative…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS - Presence of Acetobacter nitrogenifigens bacteria.

Cause type: Microbial contamination

Bacteria, mold, yeast or other microorganisms detected in the product. Contamination can occur from water systems, equipment or handling, and can cause infection. All microbial contamination recalls.

What was recalled

Freskaro refresh & revitalize Magnesium Citrate Saline Laxative Oral Solution Grape Flavor 10 fl. oz, Manufactured by: Pharma Lobis, 7400 Alumax Dr., Texarkana, TX 75501, NDC 82645-311-10.

Affected NDC 82645-0311-10

Compare with the code on your package — it is the most precise check available.

Drug: Magnesium

Product details

From the FDA NDC directory, for the product code this recall names. Compare with the label on your package.

ProductStrengthForm & routeLabelerType
Magnesium Citrate
Freskaro Magnesium Citrate Oral Solution - Grape
NDC 82645-0311
MAGNESIUM CITRATE 1.745 g/29.6mL Liquid
Oral
Pharma Nobis, LLC OTC
Recalling firm
Pharma Nobis LLC
NDC code
82645-311-10
Origin
TX, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0230-2024 · FDA notice

Check, then ask. Class II means harm is possible but usually temporary or reversible. Find the lot number on your package; if it matches, ask your pharmacist about a replacement. Do not simply stop a prescribed medication on your own - the gap can be riskier than the recall.

Other Magnesium recalls

See all
Class I · High risk

Magnesium Sulfate in Water for Injection

Product mix up: a foil pouch labeled "Magnesium Sulfate in Water for Injection, 4 g/100 mL" actually contained an IV bag of Tranexamic Acid instead.

Ongoing Labeling / mix-up Amneal Pharmaceuticals, LLC NDC 70121-1720-3 D-0478-2026

Other recalls by Pharma Nobis LLC

All 2023 recalls