SANDIMMUNE Oral Solution (cyclosporine oral solution, USP) 100 mg/mL, 50 mL bottle, Rx Only, Manufactured by: DELPHARM Huningue S.A.S., Huningue, France, Distributed by: Novartis Pharmaceuticals Corporation, East Hanover, New Jersey 07936. NDC 0078-0110-22
Class I - DangerousWhat Should You Do?
- Check if you have this product: Lot #: FX001500, FX001582, Exp. 09/30/2024
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Novartis Pharmaceuticals Corporation
- Reason for Recall:
- Crystallization: bottles of Sandimmune Oral Solution were determined to contain crystals
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- ongoing
Product Information
Full Description:
SANDIMMUNE Oral Solution (cyclosporine oral solution, USP) 100 mg/mL, 50 mL bottle, Rx Only, Manufactured by: DELPHARM Huningue S.A.S., Huningue, France, Distributed by: Novartis Pharmaceuticals Corporation, East Hanover, New Jersey 07936. NDC 0078-0110-22
Product Codes/Lot Numbers:
Lot #: FX001500, FX001582, Exp. 09/30/2024
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: D-0144-2024
Related Recalls
Crystallization: bottles of Sandimmune Oral Solution were determined to contain crystals.
Neoral soft gelatin capsules (cyclosporine capsules, USP) Modified, 25 mg, Rx Only, 30 Soft Gelatin Capsules per carton, Mfg by: Novartis Pharmaceuticals Corporation, East Hanover, NJ 07936, NDC # 0078-0246-15.
Novartis Pharmaceuticals
CGMP deviations: Out of specification results obtained during routine stability testing for ethanol content.
Failed Impurities/Degradation Specifications.