Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
RxRecalls Get alerts
Class I · High risk Terminated Initiated Jul 15, 2022 (4 years ago)

EQUALINE magnesium citrate saline laxative

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Microbial contamination of non-sterile products.

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

EQUALINE magnesium citrate saline laxative, oral solution, (1.745 g/fl oz), DYE FREE lemon flavor, 10 FL OZ (296 mL), Distributed by Supervalu Inc. Eden Prairie, MN 55344 USA, or Distributed By UNFI Providence, RI 02908, NDC 41163-769-38 UPC 0 41163 50068 6

Affected NDC 41163-0769-38

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
citroma
Magnesium Citrate
NDC 41163-0769
1.745 g/29.6mL Liquid
Oral
United Natural Foods, Inc. dba UNFI OTC
Recalling firm
Vi-Jon, LLC
NDC code
41163-769-38
Origin
TN, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1502-2022 · FDA notice

Treat this as urgent. Class I means FDA judged there is a reasonable probability of serious harm. Find the lot number on your package; if it matches the recalled lots, do not take another dose before you have spoken to your pharmacist or prescriber - today, not next week. This recall is now terminated, which means the firm has finished removing the affected product; anything on pharmacy shelves today should be unaffected.

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 Vi-Jon, LLC

All 2022 recalls