RAPIDPOINT 500 10697306

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2016-05-04 for RAPIDPOINT 500 10697306 manufactured by Siemens Healthcare Diagnostics.

Event Text Entries

[44899097] Siemens is in process of evaluating the event. The root cause for the event is unknown.
Patient Sequence No: 1, Text Type: N, H10


[44899098] Customer reported discordant sodium and potassium results on the instrument. There was no report of injury due to this event.
Patient Sequence No: 1, Text Type: D, B5


[48200005] Siemens investigated the issue. From the data received, it appears that the sodium and potassium sensors were functioning properly. There is no evidence that the sensors were malfunctioning since there was only 1 potassium drift and 3 sodium drifts all of which did not occur on the days of the events. In both incidences on (b)(6), the patient sample had higher recovery for sodium, potassium, and chloride on system (b)(4) than on system (b)(4). Also, glucose and lactate recoveries were lower on system (b)(4) than on system (b)(4). This is consistent with contamination. Most likely, sample on (b)(6) 2016 at 14:03 and sample (b)(6) 2016 at 5:32 on system 31632 were pre-analytical; most likely due to the presence of salt being introduced to the sample from the sample port/luer area ahead of the sample.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1217157-2016-00053
MDR Report Key5630036
Date Received2016-05-04
Date of Report2016-06-17
Date of Event2016-04-10
Date Mfgr Received2016-05-09
Date Added to Maude2016-05-04
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
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 Received2016-05-04
Catalog Number10697306
OperatorOTHER HEALTH CARE PROFESSIONAL
Device Availability*
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerSIEMENS HEALTHCARE DIAGNOSTICS
Manufacturer Address511 BENEDICT AVENUE TARRYTOWN 10591 US 10591


Patients

Patient NumberTreatmentOutcomeDate
10 2016-05-04

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