Fagron recalls norepinephrine injections with potential blue break-off part that could detach during use. Stop using affected lots before 2026.
Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port
Fagron recalls specific norepinephrine injections due to a risk that a blue break-off part could detach from the administration port. This could lead to contamination or injury if the part breaks off during use.
The injection contains a blue break-off part that may detach from the administration port during use. This could cause contamination or injury if the part breaks off and enters the bloodstream.
Healthcare professionals using the recalled norepinephrine injections for medical treatments. Patients receiving these injections are at risk if the break-off part detaches during administration.
Check for the product name: norepinephrine Bitartrate, 16mg per 250mL 0.9% Sodium Chloride Injection USP. Look for lot numbers C274-000049934 through C274-000051343 with expiration dates up to May 2026.
Immediately stop using the recalled norepinephrine injections if you have them.
Ask your healthcare provider for instructions on how to safely dispose of or replace the affected product.
The recalled product is norepinephrine Bitartrate, 16mg per 250mL 0.9% Sodium Chloride Injection USP from Fagron Sterile Services with specific lot numbers and expiration dates.
Check the product label for lot numbers C274-000049934 through C274-000051343 with expiration dates up to May 2026.
Immediately stop using the product and contact your healthcare provider for instructions on safe disposal or replacement.
We’ve drafted a message you can send Fagron to request your refund or repair — edit it as you like.
Subject: Recall D-0438-2026 — Fagron Fagron Hello, I own a Fagron that is covered by recall D-0438-2026 from Fagron. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
