ADVIA CENTAUR XP 078-A010

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,05,06 report with the FDA on 2015-02-22 for ADVIA CENTAUR XP 078-A010 manufactured by Siemens Healthcare Diagnostics, Inc..

Event Text Entries

[17574544] Smoke emission was detected from the advia centaur xp direct water feed tubing. The fire department was contacted, who checked the laboratory. There was no report of injury to staff, damage to property or impact to patients.
Patient Sequence No: 1, Text Type: D, B5


[17700703] A siemens customer service engineer (cse) was dispatched to the customer site. After evaluation of the instrument and instrument data, the cse determined the 2-way solenoid valve malfunctioned. The 2-way solenoid valve is connected to the direct water feed tubing. The cse determined the 2-way solenoid valve over-heated and caused the smoke emission. The cse replaced the 2-way solenoid valve. The instrument is performing within specifications. Further evaluation of the device is not required.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2432235-2015-00089
MDR Report Key4533313
Report Source01,05,06
Date Received2015-02-22
Date of Report2015-01-29
Date of Event2015-01-28
Date Mfgr Received2015-01-29
Device Manufacturer Date2010-05-14
Date Added to Maude2015-03-25
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional0
Initial Report to FDA3
Report to FDA3
Event Location0
Manufacturer ContactJOHN NELSON
Manufacturer Street511 BENEDICT AVENUE
Manufacturer CityTARRYTOWN NY 10591
Manufacturer CountryUS
Manufacturer Postal10591
Manufacturer Phone9145242530
Manufacturer G1SIEMENS HEALTHCARE DIAGNOSTICS
Manufacturer StreetMANUFACTURING LIMITED REGISTRATION NUMBER: 8020888
Manufacturer CityCHAPEL LANE, SWORDS CO DUBLIN,
Manufacturer CountryEI
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameADVIA CENTAUR XP
Generic NameIMMUNOASSAY ANALYZER
Product CodeMOI
Date Received2015-02-22
Model NumberADVIA CENTAUR XP
Catalog Number078-A010
ID NumberN/A
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerSIEMENS HEALTHCARE DIAGNOSTICS, INC.
Manufacturer Address511 BENEDICT AVENUE TARRYTOWN NY 10591 US 10591


Patients

Patient NumberTreatmentOutcomeDate
10 2015-02-22

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