Class III · Low risk Ongoing
Magnesium Chloride
Reason Subpotent drug
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.
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
- 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
What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.
Other Magnesium recalls
See all
Class I · High risk Ongoing
Magnesium Sulfate in Water for Injection
Reason 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.
Class II · Moderate risk Ongoing
INON ACE Antacid tablets
Reason Failed Disintegration Specifications: above the time expected.
Class II · Moderate risk Ongoing
Magnesium Chloride for Injection
Reason Lack of Assurance of Sterility
Class II · Moderate risk Ongoing
Glutathione Magnesium for Injection
Reason Lack of Assurance of Sterility
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