Fresenius recalls Citrasate Liquid Acid concentrate bottles (Model 08-3251-CA) used in hemodialysis machines due to low sodium/calcium levels. Affected lot numbers: 20LXAC051.
The sodium and/or calcium levels in these concentrates were below the manufacturing specifications.
Fresenius is recalling Citrasate Liquid Acid concentrate bottles (Model 08-3251-CA) used in hemodialysis machines because the sodium and calcium levels were below manufacturing specifications. This could lead to improper treatment and health risks for patients using the product.
The sodium and calcium levels in the concentrate were too low, which could cause improper dialysis treatment. This might lead to complications like electrolyte imbalances in patients undergoing hemodialysis.
Patients using hemodialysis machines with this specific Citrasate Liquid Acid concentrate bottle model are affected. Those with kidney failure requiring dialysis are most at risk.
Check for the model number 08-3251-CA on the bottle. The affected lot number is 20LXAC051. This product is used with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in hemodialysis machines.
Look for the model number 08-3251-CA and lot number 20LXAC051 on the bottle.
The product was recalled because sodium and calcium levels were below specifications, but it may still be safe for use if the levels are corrected through proper dialysis procedures.
Check for the model number 08-3251-CA and lot number 20LXAC051 on the bottle. This product is used with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in hemodialysis machines.
The recall record does not specify a remedy, so contact Fresenius Medical Care Holdings, Inc. for guidance.
We’ve drafted a message you can send Fresenius to request your refund or repair — edit it as you like.
Subject: Recall Z-0827-2021 — Fresenius Fresenius Hello, I own a Fresenius that is covered by recall Z-0827-2021 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.
