Fresenius recalls NaturaLyte Liquid Acid concentrate drums (Model 13-2251-0) used in hemodialysis machines due to low sodium/calcium levels. Affected lots listed; check your product for specific lot numbers.
The sodium and/or calcium levels in these concentrates were below the manufacturing specifications.
Fresenius Medical Care recalls NaturaLyte Liquid Acid concentrate drums (Model 13-2251-0) used in hemodialysis machines because they may have sodium and calcium levels below required specifications. This could affect the safety of the dialysis treatment if the concentrates are used without proper dilution.
The concentrates may have sodium and calcium levels below the required manufacturing specifications. This could lead to improper dialysis treatment if the concentrates are not diluted correctly, potentially affecting patient health.
Patients using hemodialysis machines with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution system. Healthcare providers handling these specific drums are most at risk.
Check for the model number 13-2251-0 on the drum. Affected lots include specific numbers listed in the recall notice, such as 20LXAC070, 20LXAC103, and others.
Identify the lot number on the drum to see if it matches the affected lots listed in the recall notice.
The model number is 13-2251-0.
Patients using hemodialysis machines with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution system.
Check the lot number on the drum against the list of affected lots provided in the recall notice.
We’ve drafted a message you can send Fresenius to request your refund or repair — edit it as you like.
Subject: Recall Z-0825-2021 — Fresenius Fresenius Hello, I own a Fresenius that is covered by recall Z-0825-2021 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
