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 2015-10-28 for RAPIDPOINT 405 10320055 manufactured by Siemens Healthcare Diagnostics.

Event Text Entries

[30063022] Siemens representative gave customer instructions how to edit the sample in recall/patients/edit. Customer edited the id# and printed result to transmit to rapid comm. Customer indicated that incorrect patient id was a typo. The event has occurred due to an operator error. Instrument is performing as intended.
Patient Sequence No: 1, Text Type: N, H10


[30063023] Customer reported that they entered incorrect patient id# for a patient sample. Customer indicated that patient id was entered manually and they wanted to know how to correct it. Customer indicated that result was not released or reported to physician. There was no report of injury due to this event.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1217157-2015-00150
MDR Report Key5185165
Date Received2015-10-28
Date of Report2015-10-28
Date of Event2015-10-07
Date Mfgr Received2015-10-07
Date Added to Maude2015-10-28
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationRESPIRATORY THERAPIST
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 Report0

Device Details

Brand NameRAPIDPOINT 405
Generic NameRP 405
Product CodeGKR
Date Received2015-10-28
Catalog Number10320055
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 2015-10-28

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