FDA Recall D-0488-2026
Avantor Performance Materials LLC · Paris, KY
Class III Ongoing 44 days on record
Lower impact — Class III recall — product violates FDA labeling or manufacturing standards but is unlikely to cause adverse health consequences.
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 for recall
Subpotent drug
Recall record
- Recall number
D-0488-2026- Classification
- Class III
- Status
- Ongoing
- Voluntary or mandated
- Voluntary: Firm initiated
- Firm notification
- Letter
- Distribution
- Nationwide in the USA, Belgium and France
- Recall initiated
- 2026-03-31
- Classified by FDA Center
- 2026-04-22
- FDA published
- 2026-04-22
- Recalling firm
- Avantor Performance Materials LLC
- Firm location
- Paris, KY
Operational response
Class III recalls are unlikely to cause adverse health consequences but indicate a violation of FDA labeling or manufacturing standards. Pull from active dispensing per your operational policy.
For the official FDA enforcement record, see FDA's Recall Search.