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DRUG RECALLMODERATE
Nomida Semaglutide Injection
Nomida is recalling Semaglutide Injection 2 mg vials (NDC 84223-001-06) due to a lack of assurance of sterility.
What to do
Stop using this product immediately and contact your healthcare provider for an alternative treatment. Return the product to the place of purchase or contact New Life Pharma LLC for further instructions.
Why it was recalled
Lack of Assurance of Sterility
How to identify it
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
Where it was sold
Distributed in US-OH.
Official source
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Editorial summary by Recall Canary · last updated 2026-06-05 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification