Fresenius recalls NaturaLyte Liquid Acid concentrate bottles (Model 08-2251-0) used in hemodialysis machines due to low sodium/calcium levels. Affected lots include 20LXAC048 through 20NXAC025. No remedy specified in recall notice.
The sodium and/or calcium levels in these concentrates were below the manufacturing specifications.
Fresenius Medical Care recalls NaturaLyte Liquid Acid concentrate bottles (Model 08-2251-0) used with hemodialysis machines because the sodium and calcium levels were too low. This could lead to improper treatment during kidney dialysis. The recall affects specific production lots.
The concentrates have sodium and calcium levels below the required manufacturing standards. This could cause inadequate dialysis treatment if used in hemodialysis machines, potentially leading to complications for patients with kidney failure.
Patients using hemodialysis machines with Fresenius Renal Technologies Sodium Bicarbonate Concentrate are affected. Those with the specific lot numbers listed in the recall are at risk of improper dialysis treatment.
Check the bottle for the model number 08-2251-0. The affected lots include 20LXAC048 through 20NXAC025, with additional lots added as of March 17, 2021.
Look for the lot numbers listed in the recall: 20LXAC048 through 20NXAC025, with additional lots added as of March 17, 2021.
The sodium and calcium levels in these concentrates were below the manufacturing specifications, which could lead to improper dialysis treatment.
The recall notice does not specify a remedy, so check the bottle lot number to see if it is affected and contact Fresenius for further instructions.
Yes, affected lots include 20LXAC048 through 20NXAC025, with additional lots added as of March 17, 2021.
We’ve drafted a message you can send Fresenius to request your refund or repair — edit it as you like.
Subject: Recall Z-0815-2021 — Fresenius Fresenius Hello, I own a Fresenius that is covered by recall Z-0815-2021 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.
