RAPIDPOINT 500 10492730

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,user f report with the FDA on 2016-05-02 for RAPIDPOINT 500 10492730 manufactured by Siemens Healthcare Diagnostics.

Event Text Entries

[44167324] Siemens field service engineer has installed new cartridge interface assembly and new measurement cartridge to the instrument. System is fully functional. Siemens customer product support team is in process of investigating the issue. The cause for the discordant pco2 results is unknown.
Patient Sequence No: 1, Text Type: N, H10


[44167345] Customer reported that when they run a blood sample twice on instrument, the results for pco2 didn't match. There was no report of injury due to this event.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1217157-2016-00048
MDR Report Key5624128
Report SourceCOMPANY REPRESENTATIVE,USER F
Date Received2016-05-02
Date of Report2016-05-02
Date of Event2016-04-05
Date Mfgr Received2016-04-06
Date Added to Maude2016-05-02
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationMEDICAL TECHNOLOGIST
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactSTEVEN ANDBERG
Manufacturer Street2 EDGEWATER DRIVE
Manufacturer CityNORWOOD MA 02062
Manufacturer CountryUS
Manufacturer Postal02062
Manufacturer Phone7812693655
Manufacturer G1SIEMENS HEALTHCARE DIAGNOSTICS MANUFACTURING, LTD.
Manufacturer StreetNORTHERN ROAD CHILTON INDUSTRIAL ESTATE
Manufacturer CitySUDBURY CO102XQ
Manufacturer CountryUK
Manufacturer Postal CodeCO10 2XQ
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameRAPIDPOINT 500
Generic NameRP 500
Product CodeGKR
Date Received2016-05-02
Catalog Number10492730
OperatorOTHER HEALTH CARE PROFESSIONAL
Device Availability*
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerSIEMENS HEALTHCARE DIAGNOSTICS
Manufacturer Address511 BENEDICT AVENUE TARRYTOWN 10591 US 10591


Patients

Patient NumberTreatmentOutcomeDate
10 2016-05-02

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