Norepinephrine Bitartrate recalled over sterility concerns
- Recall date
- March 20, 2026
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Fagron Compounding Services recalls norepinephrine Bitartrate, 32mg per 250mL 0.9% Sodium Chloride Injection USP, Fagron Sterile Services, 8710 34th St. N.…
- Recall number
- D-0439-2026
- FDA classification
- Class II
- Brand / firm
- Fagron Compounding Services
- Sold / distributed
- Nationwide in the U.S.A.
Why it was recalled
Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
norepinephrine Bitartrate, 32mg per 250mL 0.9% Sodium Chloride Injection USP, Fagron Sterile Services, 8710 34th St. N. Wichita, KS 67226, NDC 71266-5027-02
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