Fresenius Kabi recalls certain acyclovir sodium injections due to lack of sterility assurance. This may cause infections if used improperly. Contact the company for details.
Lack of Assurance of Sterility
Fresenius Kabi is recalling specific acyclovir sodium injections that may not be sterile. Using these products could lead to infections, especially in medical settings.
The product lacks assurance of sterility, meaning it might contain contaminants that could cause infections when administered intravenously. This is a serious risk in medical procedures where sterile conditions are critical.
Healthcare professionals and patients receiving intravenous acyclovir treatments. Those using the recalled product for medical purposes are at risk.
Check for the product name: acyclovir sodium, 200 mg, 200mg added to 100 mL, 0.9% Sodium Chloride Injection, USP, For Intravenous Use, Single-Use. The lot number C274-000049124 and expiration date 28-Feb-26 are specific identifiers.
Identify the product by checking the lot number (C274-000049124) and expiration date (28-Feb-26).
The recall states there is a lack of assurance of sterility, so it is not safe for medical use.
The recall does not specify a remedy, so contact Fresenius Kabi for further instructions.
Check the lot number (C274-000049124) and expiration date (28-Feb-26) on the product label.
We’ve drafted a message you can send Fresenius Kabi to request your refund or repair — edit it as you like.
Subject: Recall D-0333-2026 — Fresenius Kabi Fresenius Kabi Hello, I own a Fresenius Kabi that is covered by recall D-0333-2026 from Fresenius Kabi. 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.
