Fresenius Kabi recalls Sodium Acetate Injection with particulate matter that could cause serious injury. Affected lots expire through 2023. Contact for return instructions.
Presence of particulate matter: particulates composed of carbon and oxygen with varying amounts of iron and trace amounts of sodium, silicon, chromium, aluminum and cellulose.
Fresenius Kabi is recalling Sodium Acetate Injection products that contain particulate matter. This could cause serious injury if injected into the body. Patients and healthcare providers using these products should stop using them immediately.
The injection contains particulates made of carbon, oxygen, iron, and other trace elements. These particles can enter the bloodstream during injection, potentially causing serious injury or death.
Patients and healthcare providers who have received the recalled Sodium Acetate Injection products. Those using the products for medical treatments are most at risk.
Check for vials labeled 'Sodium Acetate Injection, USP, 400 mEq / 100 mL (4 mEq / mL)' in 2 trays of 20 vials per shipper. The lot numbers listed (6124193, 6124196, etc.) and expiration dates through 2023 indicate the affected products.
Immediately stop using the recalled Sodium Acetate Injection products as they contain harmful particulates that could cause serious injury.
The injection contains particulate matter made of carbon, oxygen, iron, and other trace elements that could cause serious injury if injected.
Lots 6124193, 6124196, 6124226, 6125333, 6125678, and 6126846 with expiration dates through 2023.
Look for vials labeled 'Sodium Acetate Injection, USP, 400 mEq / 100 mL (4 mEq / mL)' in 2 trays of 20 vials per shipper with the listed lot numbers.
We’ve drafted a message you can send Fresenius Kabi to request your refund or repair — edit it as you like.
Subject: Recall D-0750-2022 — Fresenius Kabi Fresenius Kabi Hello, I own a Fresenius Kabi that is covered by recall D-0750-2022 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.
