NxStage recalls specific lots of PureFlow B Solution for hemodialysis that may burst, causing injury if electrolyte fluid contacts skin or eyes. Affected units include lots F1708230-F1711345 and Q1711844-Q1804888.
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 is recalling specific lots of PureFlow B Solution for hemodialysis because a smaller chamber in the bag can burst, potentially causing injury if electrolyte fluid contacts skin or eyes. This is a serious hazard for patients using hemodialysis treatments.
The smaller chamber in the PureFlow B Solution bag can burst, releasing electrolyte fluid that may cause injury if it contacts skin or eyes. This risk occurs during normal use when the solution is handled or administered.
Patients using hemodialysis treatments with the recalled PureFlow B Solution lots are most at risk. Healthcare providers and dialysis centers that use these specific lots should also stop using them immediately.
Check the lot number on the bag. The recalled lots include F1708230 through F1711345 and Q1711844 through Q1804888. The product is used for hemodialysis treatments.
Immediately stop using the recalled PureFlow B Solution lots to prevent potential injury from burst chambers.
The smaller chamber in the PureFlow B Solution bag can burst, releasing electrolyte fluid that may cause injury if it contacts skin or eyes.
Affected lots include F1708230, F1708231, F1708234, F1708235, F1708237, F1708245, F1708246, F1708247, F1708250, F1708251, F1708253, F1708254, F1708256, F1709260, F1709261, F1709267, F1710327, F1710328, F1711343, F1711344, F1711345, Q1711844, Q1711853, Q1711854, Q1711855, Q1712025, Q1712091, Q1712092, Q1712137, Q1801146, Q1801147, Q1801148, Q1801149, Q1801151, Q1801202, Q1801221, Q1801225, Q1801226, Q1801335, Q1801336, Q1801337, Q1801338, Q1801339, Q1801340, Q1802507, Q1802508, Q1802509, Q1802510, Q1802511, Q1802512, Q1803685, Q1803686, Q1803687, Q1803690, Q1803750, Q1803754, Q1803755, Q1803774, Q1803775, Q1803776, Q1803847, Q1803848, Q1803849, Q1804888.
Check the lot number on the bag. The recalled lots include F1708230 through F1711345 and Q1711844 through Q1804888.
We’ve drafted a message you can send NxStage to request your refund or repair — edit it as you like.
Subject: Recall Z-0504-2019 — NxStage NxStage Hello, I own a NxStage that is covered by recall Z-0504-2019 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
