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Class IIIOngoing

Magnesium Chloride recall

FDA recall D-0488-2026 · initiated Mar 31, 2026

By the pharmaranks editorial teamReviewed against the FDA (openFDA) sourcesUpdated Apr 22, 2026How we research

Avantor Performance Materials LLC recalled Magnesium Chloride in Mar 2026 — an FDA Class III recall (D-0488-2026) because Subpotent drug.

Unlikely to cause harm but violates FDA labeling or manufacturing regulations.

Why it was recalled

Subpotent drug

Wrong strength, or it did not keep

The product did not contain what the label promised, or stopped meeting specification before its expiry date. Under-strength medicine can mean an untreated condition.

This is a manufacturing or quality failure, not a finding that the medicine is unsafe to take — across every recall we hold, none was issued for that reason. It does not mean the batch was harmless.

Is your product affected? Check the lot number

A recall covers only specific lots. Find the lot number and expiration date on your package and compare them to the affected codes below — if yours is not listed, it was not part of this recall.

Lot 23G3161005, Exp 9/21/2027

Quantity recalled: 36 bottles

Details

Product
Magnesium Chloride, 6-Hydrate, Crystal, 500G per bottle, Bulk active pharmaceutical ingredient (API), Avantor Performance Materials, LLC, 100 Matsonford Road, Suite 200, Radnor, PA 19087, NDC 10106-2448-1
Recalling company
Avantor Performance Materials LLC
Classification
Class III
Status
Ongoing
Type
Voluntary: Firm initiated
Distribution
Nationwide in the USA, Belgium and France
Initiated
Mar 31, 2026
FDA report date
Apr 22, 2026
What to do.If you have a recalled product, don't throw away questions — check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This page reproduces public FDA data and is not medical advice.

Frequently asked

Was Magnesium Chloride recalled?
Avantor Performance Materials LLC recalled Magnesium Chloride in Mar 2026 — an FDA Class III recall (D-0488-2026) because Subpotent drug. Unlikely to cause harm but violates FDA labeling or manufacturing regulations.
Why was Magnesium Chloride recalled?
Per the FDA enforcement record, the reason for recall D-0488-2026 was: Subpotent drug
Is a recalled Magnesium Chloride dangerous to take?
An FDA recall removes specific lots from the market for a defined reason and does not by itself mean the medicine is unsafe for everyone — your specific lot may never have been affected. Unlikely to cause harm but violates FDA labeling or manufacturing regulations. Check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This reproduces public FDA data and is not medical advice.
Which lots of Magnesium Chloride are affected?
Distributed: Nationwide in the USA, Belgium and France. The recall covers these lots — Lot 23G3161005, Exp 9/21/2027. Check the lot number and expiration date on your package against this list; if yours is not listed, it was not part of recall D-0488-2026.

Source: openFDA Drug Enforcement record D-0488-2026

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