← FDA ENFORCEMENT
D-1174-2023Class I

Novartis Pharmaceuticals Corp.

Recalling firm
Novartis Pharmaceuticals Corp.
Product type
Drug
Status
Ongoing
Report date
2023-09-27
Distribution
Nationwide in the USA
Firm state
NJ
Product quantity
1272 bottles
Initiated by
Voluntary: Firm initiated
Reason for recall

Crystallization: bottles of Sandimmune Oral Solution were determined to contain crystals.

Product 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.

Code / lot info

FX001691, Exp. 12/31/2025

Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.