NxStage recalls PureFlow B Solution (lot Q1811792) due to mislabeling with incorrect product numbers. This may cause confusion in hemodialysis treatments. Affected units should be checked for lot numbers.
Certain lots were mislabeled with incorrect product number.
NxStage is recalling a specific lot of PureFlow B Solution used in hemodialysis treatments because it was mislabeled with the wrong product number. This could lead to confusion in treatment setups if the incorrect product is used.
The solution was mislabeled with an incorrect product number, which could cause confusion during hemodialysis treatments. This might lead to using the wrong product in the treatment setup, potentially affecting patient safety.
Hemodialysis patients using NxStage PureFlow B Solution with lot number Q1811792 are affected. Healthcare providers who use this product for renal replacement therapy are at risk of using the wrong product.
Check the lot number on the product label. The affected lot is Q1811792, which expires November 1, 2020. This product is used with renal replacement therapy systems for hemodialysis.
Look for the lot number Q1811792 on the PureFlow B Solution container.
The product was mislabeled with an incorrect product number, which could cause confusion in hemodialysis treatments.
Check the lot number on the product label. If it is Q1811792, contact NxStage Medical Inc for guidance.
The product is safe to use if the correct lot number is verified. Mislabeling could lead to using the wrong product in treatment.
We’ve drafted a message you can send NxStage to request your refund or repair — edit it as you like.
Subject: Recall Z-1706-2019 — NxStage NxStage Hello, I own a NxStage that is covered by recall Z-1706-2019 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.
