Skip to content
Recall Observatory FDA recall evidence

Device product

NxStage PureFlow B Solution-RFP-406, Premixed Dialysate for Hemodialysis NxStage PureFlow B Solution is indicated for use with renal replacement therapy systems that utilize sterile premixed dialysate during hemodialysis.

Z-0505-2019

October 17, 2018

Class II

Product summary

Firm
NxStage Medical, Inc.
Event
Event 81445
Status
Terminated
Classification
Class II
Quantity
16585
Official record key
device-enforcement:Z-0505-2019

Official wording

Reason: 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

Code information: Lot Numbers: F1710314, Q1712034, Q1801223, Q1801224, Q1801344, Q1802451, Q1803684, Q1803817, Q1804904

Distribution pattern: US Nationwide Distribution.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    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