FDA Adverse Event Malfunction Summary report: N

NXSTAGE SYSTEM ONE

MDR report key: 23714698 · Received December 4, 2025

Report

Report Number
3003464075-2025-00124
Event Type
Malfunction
Date Received
December 4, 2025
Date of Event
November 7, 2025
Report Date
December 4, 2025
Manufacturer
NXSTAGE MEDICAL, INC.
Product Code
FKR
PMA / PMN Number
K111174
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
003

Narratives

Additional Manufacturer Narrative · 0

THE DEVICE WAS NOT RECEIVED FOR EVALUATION. THE NXSTAGE SYSTEM ONE USER GUIDE OUTLINES RISKS ASSOCIATED WITH PERFORMING HEMODIALYSIS THERAPY AND WARNS ALL TREATMENTS MUST BE ADMINISTERED UNDER A PHYSICIAN'S PRESCRIPTION AND MUST BE PERFORMED BY A TRAINED AND QUALIFIED PERSON, CONSIDERED TO BE COMPETENT IN THE USE OF THIS DEVICE BY THE PRESCRIBING PHYSICIAN. THE DEVICE MEETS REQUIREMENTS FOR ELECTRICAL AND SAFETY STANDARDS AS OUTLINED IN THE NXSTAGE PUREFLOW USER GUIDE. PER THE NXSTAGE PUREFLOW USER GUIDE, PROPER ELECTRICAL HOOKUP IN FULL COMPLIANCE WITH ALL APPLICABLE CODES AND DEVICE SPECIFICATIONS MUST BE MAINTAINED. UDI: (B)(4).

Description of Event or Problem · 0

A REPORT WAS RECEIVED ON 07 NOV 2025 FROM A 63-YEAR-OLD MALE PATIENT WITH A MEDICAL HISTORY INCLUDING END STAGE RENAL DISEASE, WHO STATED HIS DEVICE SMELLED LIKE SMOKE AND TRIPPED THE CIRCUIT BREAKER AT HIS HOME WHILE MAKING A BATCH OF DIALYSATE ON (B)(6) 2025. ADDITIONAL INFORMATION WAS RECEIVED ON 18 AND 24 NOV 2025 FROM THE HOME THERAPY NURSE (HTN) WHO STATED THE PATIENT OBSERVED SPARKS COMING FROM THE DEVICE IN ADDITION TO A ¿POPPING SOUND¿, AND THE SMELL OF SMOKE. PER THE HTN, NO OPEN FLAME WAS PRESENT AND THERE WAS NO ADVERSE IMPACT TO THE PATIENT WHO CONTINUES TO PERFORM THERAPY WITH NXSTAGE SYSTEM.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2744256 NXSTAGE SYSTEM ONE HIGH PERMEABILITY HEMODIALYSIS SYSTEM FKR NXSTAGE MEDICAL, INC. NX2000-1

Patients

Seq Age Sex Outcome Treatment
1 63 YR Male Other