Fagron recalls specific Vancomycin HCI injections due to risk of blue break-off part detaching from administration port, potentially causing infection. Affected lots and expiration dates listed.
Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port
Fagron recalls certain Vancomycin injections because a blue break-off part could detach from the administration port, risking infection. Patients using these products should stop using them immediately.
The blue break-off part could detach from the administration port during use, potentially causing infection or contamination of the injection site. This risk exists even with proper handling and storage.
Patients receiving Vancomycin injections from Fagron Sterile Services in the US. Those with the specific lot numbers and expiration dates listed are most at risk.
Check the product label for the lot numbers: C274-000050858 (exp. 7/6/2026), C274-000051018 (exp. 7/13/2026), and other listed lots. The product is a Vancomycin HCI injection with 1.5 grams added to 250 mL of 0.9% Sodium Chloride Injection USP.
Immediately stop using the recalled Vancomycin injections if you have them.
A blue break-off part could detach from the administration port, potentially causing infection or contamination.
Lots C274-000050858 (exp. 7/6/2026), C274-000051018 (exp. 7/13/2026), and other specific lots listed in the recall.
Check the product label for the lot numbers listed in the recall: C274-000050858, C274-000051018, and others with specific expiration dates.
We’ve drafted a message you can send Fagron to request your refund or repair — edit it as you like.
Subject: Recall D-0441-2026 — Fagron Fagron Hello, I own a Fagron that is covered by recall D-0441-2026 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
