Baxter Healthcare Corporation recalls Dianeal Low Calcium (2.5 mEq/L) Peritoneal Dialysis Solution with 2.5% Dextrose, For Intraperitoneal Administration
Baxter recalls Dianeal Low Calcium (2.5 mEq/L) peritoneal dialysis solution with 2.5% dextrose due to potential leaks from connector assembly. This could risk infection during dialysis. Check NDC 0941-0457-01 and lot R24B25FA.
Use caution until it’s fixed
Lack of Assurance of Sterility: Potential presence of leaks originating from the Connector Assembly component.
Contact the company & request your remedy
What happened, in plain English
Baxter is recalling Dianeal Low Calcium peritoneal dialysis solution because it may have leaks in the connector assembly, which could lead to infection during dialysis. Patients using this product should stop using it and contact Baxter for guidance. Read more at govinfonow.com/recall/32630-baxter-dianeal-low-calcium-peritoneal-dialysis-solution-recall-potential-sterility.
Source Summary by GovInfoNow · govinfonow.com/recall/32630-baxter-dianeal-low-calcium-peritoneal-dialysis-solution-recall-potential-sterility · Updated September 23, 2026 · FDA enforcement record: FDA #D-0587-2024
Cite this page
“Baxter Dianeal Low Calcium Peritoneal Dialysis Solution Recall: Potential Sterility Issues.” GovInfoNow, updated September 23, 2026. https://govinfonow.com/recall/32630-baxter-dianeal-low-calcium-peritoneal-dialysis-solution-recall-potential-sterility. Based on FDA recall #D-0587-2024 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0587-2024%22&limit=1).
Why it’s dangerous
The connector assembly in this dialysis solution may leak, creating a risk of infection during peritoneal dialysis. This is a serious concern because the solution is used directly in the abdomen, and leaks could introduce bacteria.
Who’s affected
People using peritoneal dialysis with this specific solution are affected. Those with compromised immune systems or recent dialysis procedures are at higher risk.
How to tell if you have this one
Check for the NDC code 0941-0457-01 and lot number R24B25FA on the product label. This solution is only available by prescription and sold in 6000 mL bags.
- Brand
Baxter Healthcare- Category
Drug
What to do — step by step
Stop Using It Now
If you have the recalled solution, stop using it immediately to prevent potential infection.
Questions people ask
Is this product safe to use?
No, the product has been recalled due to potential leaks that could cause infection. Do not use it.
How can I check if I have the recalled product?
Look for the NDC code 0941-0457-01 and lot number R24B25FA on the product label.
What should I do if I have the recalled product?
Stop using it immediately and contact Baxter Healthcare for further instructions.
Contact Baxter Healthcare
We’ve drafted a message you can send Baxter Healthcare to request your refund or repair — edit it as you like.
Subject: Recall D-0587-2024 — Baxter Healthcare Baxter Healthcare Hello, I own a Baxter Healthcare that is covered by recall D-0587-2024 from Baxter Healthcare. 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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Where this comes from
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.
- Official source: FDA Recall #D-0587-2024 (June 17, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0587-2024 to see it in context.
- Plain-language summary written by qwen3:4b on September 23, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.