NxStage PureFlow B Solution Recall: Small Chamber Burst Risk

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Contact the company & request your remedy

Recalling firmNxStage Medical, Inc.350 Merrimack St, N/A · Lawrence, MA 01843-1748

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

NxStage is recalling certain lots of PureFlow B Solution for hemodialysis. The small chamber in the solution bag can burst, causing injury if it contacts skin or eyes.

Why it’s dangerous

The small chamber in the solution bag can burst, releasing electrolyte fluid that may cause injury if it contacts skin or eyes. This is a risk during hemodialysis treatment.

Who’s affected

Hemodialysis patients using the recalled lots of PureFlow B Solution are most at risk. The product is used for kidney treatment.

How to tell if you have this one

Check the lot number on the bag: F1708255, F1709265, F1710323, Q1711861, Q1711863, Q1712021, Q1712022, Q1712023, Q1712033, Q1801345, Q1802399, Q1802400.

Brand
NxStage
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Lot Number
Look for the lot numbers listed: F1708255, F1709285, F1710323, Q1711861, Q1711863, Q1712021, Q1712022, Q1712023, Q1712033, Q1801345, Q1802399, Q1802400.

✎ GovInfoNow

Questions people ask

What is the hazard with this product?

The small chamber in the solution bag can burst, releasing electrolyte fluid that may cause injury if it contacts skin or eyes.

How can I tell if I have the recalled product?

Check the lot number on the bag: F1708255, F1709285, F1710323, Q1711861, Q1711863, Q1712021, Q1712022, Q1712023, Q1712033, Q1801345, Q1802399, Q1802400.

What should I do if I have the recalled product?

The recall record does not specify a remedy, so contact NxStage for instructions.

Take action

Contact NxStage

We’ve drafted a message you can send NxStage to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-0502-2019 — NxStage NxStage

Hello,

I own a NxStage that is covered by recall Z-0502-2019 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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Where this comes from

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.

Official source: FDA Recall #Z-0502-2019 (October 17, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0502-2019 to see it in context.
Plain-language summary written by qwen3:4b on August 20, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

NxStage Medical, Inc. recalls NxStage PureFlow B Solution-RFP-402, Premixed Dialysate for Hemodialysis NxStage PureFlow B Solution is indicated for

Use caution until it’s fixed