RAPIDPOINT 405 10320055

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2016-09-15 for RAPIDPOINT 405 10320055 manufactured by Siemens Healthcare Diagnostics.

Event Text Entries

[55219572] Based on the data, the na+ and cl- both experienced a calibration drift after this sample was run on the rp405 instrument. The customer was asked if lithium heparin blood collection device was used to collect the specimen. They confirmed that in fact na heparin was used which would increase the sodium concentration of the specimen. Note there are periods during use life where there is evidence of benzalkonium in use. Benzalkonium is a known interferent on the rapidpoint 400/405/500 na+ sensor. The source of this substance should be located and removed to avoid this contamination. The instrument is performing as intended.
Patient Sequence No: 1, Text Type: N, H10


[55219573] The customer suspected a discordant sodium (na+) result on one patient sample on rp405 sn (b)(4) vs. The main laboratory result run on a gem4000. There was no report of injury due to this event.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1217157-2016-00105
MDR Report Key5953382
Date Received2016-09-15
Date of Report2016-09-15
Date of Event2016-08-25
Date Mfgr Received2016-08-30
Date Added to Maude2016-09-15
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
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
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 INDUSTRY
Manufacturer CitySUDBURY CO102XQ
Manufacturer CountryUK
Manufacturer Postal CodeCO10 2XQ
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameRAPIDPOINT 405
Generic NameRP 405
Product CodeGKR
Date Received2016-09-15
Catalog Number10320055
OperatorNURSE
Device AvailabilityY
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerSIEMENS HEALTHCARE DIAGNOSTICS
Manufacturer Address511 BENEDICT AVENUE TARRYTOWN NY 10591 US 10591


Patients

Patient NumberTreatmentOutcomeDate
10 2016-09-15

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