Fresenius Medical Care recalls NaturaLyte Liquid Acid concentrate bottles (Model 08-1251-1) due to low sodium/calcium levels. These bottles are used with Fresenius hemodialysis machines. Affected lots include 20NXAC005, 20LXAC098, and others. Contact for remedy.
The sodium and/or calcium levels in these concentrates were below the manufacturing specifications.
Fresenius Medical Care recalls NaturaLyte Liquid Acid concentrate bottles (Model 08-1251-1) because they may have sodium and calcium levels below the required specifications. This could affect the safety of hemodialysis treatments if used with Fresenius Renal Technologies machines.
The bottles may contain sodium and calcium levels below what the manufacturer intended. This could lead to improper dialysis treatment if used in the specified hemodialysis machine setup.
Patients using hemodialysis with Fresenius Renal Technologies machines who use these specific NaturaLyte bottles. Those with kidney failure requiring dialysis are most at risk.
Check for Model Number 08-1251-1 on the bottle. These bottles are used with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in hemodialysis machines. Affected lots include 20NXAC005, 20LXAC098, 20NXAC037, 20NXAC039, and others listed in the recall.
Look for Model Number 08-1251-1 on the bottle to confirm it is affected.
The sodium and/or calcium levels in these concentrates were below the manufacturing specifications.
The recall does not specify a remedy, so contact Fresenius Medical Care for guidance.
Affected lots include 20NXAC005, 20LXAC098, 20NXAC037, 20NXAC039, and additional lots listed as of March 17, 2021.
We’ve drafted a message you can send Fresenius Medical Care to request your refund or repair — edit it as you like.
Subject: Recall Z-0811-2021 — Fresenius Medical Care Fresenius Medical Care Hello, I own a Fresenius Medical Care that is covered by recall Z-0811-2021 from Fresenius Medical Care. 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.
