Fresenius recalls NaturaLyte Liquid Acid concentrate bottles (Model 08-2231-2) due to low sodium and calcium levels. These bottles are used in hemodialysis machines. Affected units have Lot Number 20NXAC034.
The sodium and/or calcium levels in these concentrates were below the manufacturing specifications.
Fresenius is recalling NaturaLyte Liquid Acid concentrate bottles (Model 08-2231-2) because they may have sodium and calcium levels below the required specifications. This could affect the safety of hemodialysis treatments if used in compatible dialysis machines.
The bottles may contain sodium and calcium levels below what the manufacturer intended. This could lead to improper dialysis treatment if used in compatible hemodialysis machines, potentially affecting patient safety.
Patients using hemodialysis machines with Fresenius Renal Technologies Sodium Bicarbonate Concentrate are likely affected. Those with the specific lot number 20NXAC034 are at risk.
Check for the model number 08-2231-2 on the bottle. The lot number 20NXAC034 is associated with this recall. These bottles are used with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in hemodialysis machines.
Verify the model number (08-2231-2) and lot number (20NXAC034) on the bottle.
The sodium and calcium levels in these bottles were below the manufacturing specifications, which could affect hemodialysis treatments.
The recall record does not specify a remedy, so check the product details and contact Fresenius for further instructions.
The recall indicates potential safety issues, but the product is not explicitly unsafe for normal use. Consult Fresenius 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-0814-2021 — Fresenius Fresenius Hello, I own a Fresenius that is covered by recall Z-0814-2021 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.
