Home / Recalls / Avantor Performance Materials LLC / D-0488-2026

D-0488-2026 Class III Ongoing

Recalled by Avantor Performance Materials LLC — Paris, KY

FDA drug recall D-0488-2026 was initiated by Avantor Performance Materials LLC on Mar 31, 2026 and is designated Class III. Reason for recall: Subpotent drug The recall status is ongoing. Affected quantity: 36 bottles.

Recall Details

Product Type: Drugs
Report Date: Apr 22, 2026
Initiation Date: Mar 31, 2026
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 36 bottles

Product Description

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

Reason for Recall

Subpotent drug

Distribution Pattern

Nationwide in the USA, Belgium and France

Code Information

Lot 23G3161005, Exp 9/21/2027

Source

Dataset: openFDA drug recall enforcement reports
FDA record: This recall in openFDA (JSON)
Enforcement Report: Search FDA's Enforcement Report for D-0488-2026
openFDA file date: Nov 10, 2026
Loaded by RegDataLab: Nov 11, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.