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High risk Drugs & MedicationsClass II

Nomida Semaglutide Recall

Semaglutide Inj., 2 mg x 5, Sterile Multi-Dose Vial, Rx only, Nomida, 25055 W Valley Pkwy, Suite 106, Olathe, KS 66061, NDC 84223-001-06

Updated February 26, 2026

Nomida semaglutide 2 mg injectable vials are being recalled due to lack of assurance of sterility. Non-sterile injections can cause serious infections.

Is the New Life Pharma LLC recalled? Yes. This product was recalled by FDA on February 26, 2026. Details below.

What is recalled

Semaglutide Inj., 2 mg x 5, Sterile Multi-Dose Vial (prescription only), brand Nomida, NDC 84223-001-06, distributed by New Life Pharma LLC, 25055 W Valley Pkwy, Suite 106, Olathe, KS 66061.

Am I affected

You're affected if you have a prescription semaglutide vial labeled Nomida with NDC number 84223-001-06. Check the label on your vial for this NDC and brand name.

What to do right now

Stop using this medication immediately and contact your prescribing doctor or pharmacy. Do not use any remaining doses from the recalled vial. Your doctor will advise you on next steps and may provide a replacement or alternative treatment.

The hazard

Lack of Assurance of Sterility

Brands affected

New Life Pharma LLC
Source
FDA
Category
Drugs & Medications
Recall ID
fda-D-0393-2026
Classification
Class II
Recalled
February 26, 2026
Read the official notice

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