Fagron recalls specific Vancomycin HCL injections due to risk of blue break-off part detaching during use, 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 HCL injections because a blue break-off part could detach from the administration port, risking infection. Patients using these injections should stop using them immediately.
The blue break-off part in the injection can detach from the administration port during use. This could lead to contamination or infection if the part enters the bloodstream.
Patients receiving Vancomycin HCL injections from Fagron Sterile Services. Those with the specific lot numbers and expiration dates listed are most at risk.
Check for the product name: Vancomycin HCL, 1 gram added to 250 mL, 0.9% Sodium Chloride Injection USP. Look for the lot numbers: C274-000050987 (exp. 7/12/2026), C274-000049425 (exp. 5/2/2026), and other listed lots with specific expiration dates.
Immediately stop using the recalled Vancomycin HCL injections as they pose a risk of infection.
Vancomycin HCL, 1 gram added to 250 mL, 0.9% Sodium Chloride Injection USP from Fagron Sterile Services.
C274-000050987 (exp. 7/12/2026), C274-000049425 (exp. 5/2/2026), C274-000050069 (exp. 5/30/2026), C274-000050346 (exp. 6/10/2026), C274-000050698 (exp. 6/27/2026), C274-000050699 (exp. 6/27/2026), and C274-000050775 (exp. 7/4/2026).
The recall record states the remedy is null, meaning no specific remedy is provided beyond stopping use.
We’ve drafted a message you can send Fagron to request your refund or repair — edit it as you like.
Subject: Recall D-0442-2026 — Fagron Fagron Hello, I own a Fagron that is covered by recall D-0442-2026 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.
