Fresenius Kabi recalls Oxytocin 0.9% Sodium Chloride Injection due to cGMP violations. Affected units have specific lot numbers and expiration dates. Contact for remedy details.
cGMP violations
Fresenius Kabi is recalling Oxytocin 0.9% Sodium Chloride Injection products because of cGMP violations. This means the products may not meet quality standards and could be unsafe for medical use.
cGMP violations indicate that the manufacturing process did not follow proper quality control standards. This could lead to products that are unsafe for medical use, though the specific risk is not detailed in the recall.
Healthcare providers and patients who have received the recalled Oxytocin injection products. Those using the products for medical purposes are most at risk.
Check for the lot numbers C274-000038801 (exp. 9-Oct-24), C274-000039045 (exp. 24-Oct-24), or C274-000039240 (exp. 31-Oct-24) on the product label. The product is a single-dose bag for medical use only.
Look for the lot numbers C274-000038801, C274-000039045, or C274-000039240 on the product label.
The product was recalled due to cGMP violations, which means the manufacturing process did not meet quality standards.
The recall record does not specify a remedy, so contact Fresenius Kabi for further instructions.
The recalled products have expiration dates of 9-Oct-24, 24-Oct-24, and 31-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-0021-2025 — Fresenius Kabi Fresenius Kabi Hello, I own a Fresenius Kabi that is covered by recall D-0021-2025 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.