Class III · Lower riskActive recall
Magnesium Chloride
Unlikely to cause harm — often a labeling or packaging issue.
Does this affect you?
Check your lot numberLot 23G3161005, Exp 9/21/2027
Where it was soldNationwide in the USA, Belgium and France
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.
What happened
Subpotent drug
What to do
- Check the lot number and expiry on your medicine against the recall above.
- Talk to your pharmacist or doctor before changing anything — don't stop on your own.
- Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).
Who makes it
| Distributed by / for | Avantor Performance Materials LLC |
| NDC | 10106-2448-1 |
Show the full FDA record
| Full product label | 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 firm | Avantor Performance Materials LLC |
| Distribution | Nationwide in the USA, Belgium and France |
| Quantity | 36 bottles |
| Recall initiated | 2026-03-31 |
| Report date | 2026-04-22 |
| Recall completed | — |
| Recall number | D-0488-2026 |
| Classification | Class III |
| FDA status | Ongoing |
| Origin on file | Paris KY United States |
Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗
This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.