NxStage recalls specific lots of PureFlow B Solution for hemodialysis. Small chamber bursting may cause electrolyte fluid injury to eyes or skin. Affected lots: Q1801222, Q1801341, Q1802396, Q1802397.
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 recalls certain lots of PureFlow B Solution for hemodialysis. The smaller chamber in the bag can burst, potentially causing electrolyte fluid to contact eyes or skin and cause injury.
The smaller chamber in the PureFlow B Solution bag can burst during use. If electrolyte fluid bursts and contacts eyes or skin, it can cause injury. This is a risk during hemodialysis treatment.
Hemodialysis patients using the recalled lots of PureFlow B Solution are affected. Those with the specific lot numbers listed are most at risk.
Check the lot number on the bag: Q1801222, Q1801341, Q1802396, or Q1802397. The product is used for hemodialysis treatments.
Look for the lot number on the bag: Q1801222, Q1801341, Q1802396, or Q1802397.
The smaller chamber in the bag can burst, potentially causing electrolyte fluid to contact eyes or skin and cause injury.
Lots Q1801222, Q1801341, Q1802396, and Q1802397.
The recall does not specify a stop-use instruction; check the lot number to see if you have an affected product.
We’ve drafted a message you can send NxStage to request your refund or repair — edit it as you like.
Subject: Recall Z-0506-2019 — NxStage NxStage Hello, I own a NxStage that is covered by recall Z-0506-2019 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.
