ASAHI APS HEMODIALYZER APS1050S NA

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2004-03-15 for ASAHI APS HEMODIALYZER APS1050S NA manufactured by Nextron Medical.

Event Text Entries

[20922516] Pt experienced chills following hemodialysis therapy. Therapy was provided with a 4th-use hemodialyzer.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number518784
MDR Report Key518784
Date Received2004-03-15
Date of Report2003-12-19
Date of Event2003-11-10
Date Facility Aware2003-11-10
Report Date2003-12-19
Date Reported to Mfgr2003-12-19
Date Added to Maude2004-04-05
Event Key0
Report Source CodeUser Facility report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use0
Previous Use Code0
Event Type3
Type of Report3

Device Sequence Number: 1

Brand NameASAHI APS HEMODIALYZER
Generic NameHEMODIALYZER
Product CodeFKP
Date Received2004-03-15
Model NumberAPS1050S
Catalog NumberNA
Lot NumberUNK
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeUNKNOWN
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key507814
ManufacturerNEXTRON MEDICAL
Manufacturer Address45 KULICK RD FAIRFIELD NJ 07004 US

Device Sequence Number: 2

Brand NameRENATRON
Generic NameREPROCESSING DEVICE
Product CodeLIF
Date Received2004-03-15
Model NumberRS8330
Catalog NumberNA
Lot NumberUNK
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeUNKNOWN
Implant FlagN
Date RemovedA
Device Sequence No2
Device Event Key507816
ManufacturerMINNTECH CORP.
Manufacturer Address14605 28TH AVE NORTH MINNEAPOLIS MN 55447 US
Baseline Brand Name*
Baseline Generic NameHEMODIALZER
Baseline Model NoRS8330
Baseline Catalog NoNA
Baseline IDNA


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Other 2004-03-15

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