Celltrion Recalls One Lot of Steqeyma

August 26, 2025

The information on this site is not intended to take the place of your doctor or other healthcare professionals. It is a resource to help you make the best decisions and get the most from the medical services available to you. A licensed physician should be consulted for diagnosis and treatment of all medical conditions.

On Aug. 13, 2025, Celltrion USA initiated a recall of one lot of Steqeyma® (ustekinumab-stba) 90 mg/mL injection due to incorrect assembly and release into the market. Steqeyma is a human interleukin-12 and -23 antagonist indicated for the treatment of adult patients who have moderate to severe plaque psoriasis (PsO) and are candidates for phototherapy or systemic therapy, active psoriatic arthritis (PsA), moderately to severely active Crohn’s disease (CD) and moderately to severely active ulcerative colitis. It is also indicated for pediatric patients ages six years and older who have moderate to severe plaque psoriasis and are candidates for phototherapy or systemic therapy, as well as those who have active PsA. For more information on the recall, see here.

Last updated: August 26, 2025

The information on this site is not intended to take the place of your doctor or other healthcare professionals. It is a resource to help you make the best decisions and get the most from the medical services available to you. A licensed physician should be consulted for diagnosis and treatment of all medical conditions.