Fresenius Kabi recalls phenylephrine injection due to cGMP violations. Affected units have specific lot numbers and expiration dates. Consumers should contact the manufacturer for details.
cGMP violations
Fresenius Kabi is recalling phenylephrine injections that were produced under cGMP violations. This recall affects specific lot numbers and expiration dates, but the product is only available by prescription.
The product was made under cGMP violations, which are quality control standards for drug manufacturing. This could mean the injection may not be safe or effective for medical use.
Prescription patients who received the recalled phenylephrine injection. Healthcare providers using this product for medical treatment are most at risk.
Check the product label for the lot number C274-000037046 and expiration date 13-Oct-24. The product is a single-dose injection available by prescription only.
Reach out to Fresenius Kabi Compounding, LLC for specific instructions on handling the recalled product.
The recall indicates cGMP violations, which could affect safety and effectiveness. The manufacturer advises contacting them for details.
Contact Fresenius Kabi Compounding, LLC for specific instructions on handling the recalled product.
Check the product label for lot number C274-000037046 and expiration date 13-Oct-24.
We’ve drafted a message you can send Fresenius Kabi to request your refund or repair — edit it as you like.
Subject: Recall D-0015-2025 — Fresenius Kabi Fresenius Kabi Hello, I own a Fresenius Kabi that is covered by recall D-0015-2025 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.
