Fresenius recalls 6000mL peritoneal dialysis solution bags with potential lack of sterility. This affects patients using the product for kidney treatment. Contact Fresenius for details.
Lack of Sterility Assurance
Fresenius is recalling peritoneal dialysis solution bags that may not be sterile. This could lead to infections in patients with kidney failure who use the product. Patients should stop using these bags and contact Fresenius for a replacement.
The solution may not be sterile, which can cause infections in patients with kidney failure. Peritoneal dialysis involves direct contact with the abdomen, so contamination could lead to serious health issues.
Patients using peritoneal dialysis for kidney failure who have the recalled solution bags are affected. Those with the specific lot numbers are at highest risk.
Check for the product name 'DELFLEX Peritoneal Dialysis Solution 1.5% Dextrose' in 6000mL bags. Look for lot number 23JK02010 and expiration date 1/31/2025.
Immediately stop using the recalled peritoneal dialysis solution bags if you have them.
The recall states there is a lack of sterility assurance, so the product is not safe to use.
Check for lot number 23JK02010 and expiration date 1/31/2025 on the 6000mL bags.
Stop using the product immediately and contact Fresenius for a replacement.
We’ve drafted a message you can send Fresenius to request your refund or repair — edit it as you like.
Subject: Recall D-0218-2024 — Fresenius Fresenius Hello, I own a Fresenius that is covered by recall D-0218-2024 from Fresenius. 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.