RAPIDPOINT 405 10322347

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06,07 report with the FDA on 2015-06-11 for RAPIDPOINT 405 10322347 manufactured by Siemens Healthcare Diagnostics.

Event Text Entries

[5933587] Customer restored failed automatic quality control (aqc) parameter (po2) and run patient sample on the instrument.
Patient Sequence No: 1, Text Type: D, B5


[13366869] Customer should not have restored failed aqc parameter (po2) and run patient sample. Siemens customer care center (ccc) reviewed steps involved in setting up security level with the customer to prevent reoccurrence of this event. Customer indicated that they did not know if any treatment was performed on the patient. Customer discarded patient sample as measurement cartridge was replaced later. The event has occurred due to an operator error.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1217157-2015-00073
MDR Report Key4838173
Report Source06,07
Date Received2015-06-11
Date of Report2015-05-17
Date of Event2015-05-17
Date Mfgr Received2015-05-17
Date Added to Maude2015-07-07
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Reporter OccupationRESPIRATORY THERAPIST
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
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 405
Generic NameRP 405
Product CodeGKR
Date Received2015-06-11
Catalog Number10322347
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 2015-06-11

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