NxStage PureFlow B Solution-RFP-RFP-456 premixed dialysate for hemodialysis recalled due to risk of small chamber bursting and causing injury if electrolyte fluid contacts eyes or skin. Lot numbers F1708258, F1710322, Q1711910, Q1711911, Q1712093, Q1801227, Q1801342, Q1801343, Q1802393, Q1803816.
PureFlow B Solution smaller chamber of the two chamber bag can burst electrolyte fluid and cause injury if it comes in contact with the eyes or skin
NxStage PureFlow B Solution-RFP-RFP-456, a premixed dialysate for hemodialysis, is recalled because its smaller chamber can burst, potentially causing injury if electrolyte fluid contacts eyes or skin. This affects specific lot numbers used in hemodialysis treatments.
The smaller chamber in the solution bag can burst, releasing electrolyte fluid that may cause injury if it contacts eyes or skin. This hazard occurs during normal use when the solution is handled or administered.
Hemodialysis patients using NxStage PureFlow B Solution-RFP-RFP-456 with the affected lot numbers are most at risk. Healthcare providers administering the solution may also be affected.
Check the lot number on the bag: F1708258, F1710322, Q1711910, Q1711911, Q1712093, Q1801227, Q1801342, Q1801343, Q1802393, or Q1803816. The product is used in hemodialysis treatments for kidney failure patients.
Look for the lot number on the bag: F1708258, F1710322, Q1711910, Q1711911, Q1712093, Q1801227, Q1801342, Q1801343, Q1802393, or Q1803816.
NxStage PureFlow B Solution-RFP-RFP-456, a premixed dialysate for hemodialysis.
Lot numbers F1708258, F1710322, Q1711910, Q1711911, Q1712093, Q1801227, Q1801342, Q1801343, Q1802393, and Q1803816.
The smaller chamber in the solution bag can burst, potentially causing injury if electrolyte fluid contacts eyes or skin.
We’ve drafted a message you can send NxStage to request your refund or repair — edit it as you like.
Subject: Recall Z-0507-2019 — NxStage NxStage Hello, I own a NxStage that is covered by recall Z-0507-2019 from NxStage. 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.
