FDA Drug Recalls

Recalls / Active ingredient / Cyclosporine

Cyclosporine

7 FDA drug recalls involving the active ingredient “Cyclosporine”.

DateClassProductFirm
2023-09-07Class IIICequa (cyclosporine ophthalmic solution) 0.09%, 60 Single-Use Vials (6 pouches x 10 single-use vials (0.25 mL SUN PHARMACEUTICAL INDUSTRIES INC
2022-09-16Class IINeoral soft gelatin capsules (cyclosporine capsules, USP) Modified, 25 mg, Rx Only, 30 Soft Gelatin Capsules pNovartis Pharmaceuticals Corporation
2022-04-01Class IIICequa (cyclosporine ophthalmic solution) 0.09%, packaged in 6 pouches x 10 single-use vials (0.25 mL each) perSUN PHARMACEUTICAL INDUSTRIES INC
2021-05-07Class IIICequa (cyclosporine ophthalmic solution) 0.09%, 60 Single-Use Vials (6 pouches x 10 single-use vials (0.25 mL SUN PHARMACEUTICAL INDUSTRIES INC
2021-02-22Class IIICequa (cyclosporine ophthalmic solution) 0.09%, 60 Single-Use Vials (6 pouches x 10 single-use vials (0.25 mL SUN PHARMACEUTICAL INDUSTRIES INC
2017-02-08Class IICycloSPORINE Capsules, USP, 100 mg, 30 count (5x6) blister cartons, Rx only, Distributed by American Health PaAmerisource Health Services
2017-02-03Class IICycloSPORINE Capsules, USP, 100 mg, 30 count bottle, Rx Only, Manufactured by Apotex, Inc., Toronto, Ontario, Apotex Inc.