Fresenius recalls Citrasate Liquid Acid concentrate drums (Model 13-3251-CA) used in hemodialysis machines due to low sodium/calcium levels. Affected lots: 20LXAC032, 20NXAC003.
The sodium and/or calcium levels in these concentrates were below the manufacturing specifications.
Fresenius recalls Citrasate Liquid Acid concentrate drums used in hemodialysis machines because they may have sodium and calcium levels below required specifications. This could affect treatment safety for kidney patients using these machines.
The concentrates may have sodium and calcium levels below what manufacturers specify. This could lead to improper dialysis treatment if the machine uses these drums, potentially affecting kidney patient safety.
Kidney patients using Fresenius hemodialysis machines with these specific Citrasate Liquid Acid drums. Those with the model number 13-3251-CA and lot numbers 20LXAC032 or 20NXAC003 are most at risk.
Check for the model number 13-3251-CA on the drum. Look for lot numbers 20LXAC032 or 20NXAC003. These drums are used with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in hemodialysis machines.
Identify the model number (13-3251-CA) and lot number (20LXAC032 or 20NXAC003) on the drum.
The sodium and calcium levels may be below manufacturing specifications, which could affect dialysis treatment safety.
No, the recall does not require stopping use immediately. Check the model and lot numbers to see if your drums are affected.
Check for model number 13-3251-CA and lot numbers 20LXAC032 or 20NXAC003. These drums are used with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in hemodialysis machines.
We’ve drafted a message you can send Fresenius to request your refund or repair — edit it as you like.
Subject: Recall Z-0829-2021 — Fresenius Fresenius Hello, I own a Fresenius that is covered by recall Z-0829-2021 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.
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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.
