Magnesium Chloride Recall: Avantor Performance Materials (API)
Announced 2026-04-22 · FDA
FDA recalls Lot 23G3161005, Exp 9/21/2027, of Magnesium Chloride, 6-Hydrate, Crystal, 500G per bottle, Bulk API. The recall reason is subpotent drug. The product was distributed nationwide in the USA, Belgium, and France.
| Brand | Avantor Performance Materials LLC |
|---|---|
| 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 |
| Reason | Subpotent drug |
| Severity | low |
| Units affected | 36 |
| Distribution | Nationwide in the USA, Belgium and France |
| Agency | FDA |
WHAT YOU SHOULD DO
- Do not use any product from Lot 23G3161005.
- Contact Avantor Performance Materials or your distributor for return or disposal instructions.
- If you have used the product or have health concerns, seek medical advice.
How to identify the recalled item
| Lot / date codes | Lot 23G3161005, Exp 9/21/2027 |
|---|---|
| Lot / date codes | Lot 23G3161005, Exp 9/21/2027 |
These are the identifiers FDA published for this recall. Most recall notices list no UPC or model number at all — if the code on your item is not shown here, that does not mean the item is excluded. Check the official notice, or contact the company.
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.