ADVIA 2120I 067-A004

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06 report with the FDA on 2011-10-26 for ADVIA 2120I 067-A004 manufactured by Siemens Healthcare Diagnostics.

Event Text Entries

[19530841] The field service engineer (fse) was working on cleaning a clogged line with sodium hydroxide (naoh) on the advia 2120i hematology system. The naoh liquid splashed onto his face and his right eye. The fse rinsed his eye with cold water several times. The fse was not wearing safety glasses. The fse sought medical attention, he was examined for eye irritation but was not treated.
Patient Sequence No: 1, Text Type: D, B5


[19655206] Siemens field service engineer (fse) did not follow safety precautions when handling the hazardous liquid ( naoh) and did not wear protective safety glasses, as required. The instrument is performing within specifications. No further evaluation of the device is required.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2432235-2011-00169
MDR Report Key2309703
Report Source05,06
Date Received2011-10-26
Date of Report2011-10-21
Date of Event2011-10-21
Date Mfgr Received2011-10-21
Date Added to Maude2011-10-27
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 FDA0
Event Location0
Manufacturer ContactLINDA BARLETTA
Manufacturer Street511 BENEDICT AVE
Manufacturer CityTARRYTOWN NY 10591
Manufacturer CountryUS
Manufacturer Postal10591
Manufacturer Phone9145242299
Manufacturer G1SIEMENS HEALTHCARE DIAGNOSTICS
Manufacturer StreetMANUFACTURING LIMITED, CHAPEL LANE
Manufacturer CitySWORD, CO. DUBLIN,
Manufacturer CountryEI
Single Use3
Previous Use Code3
Removal Correction NumberN/A
Event Type3
Type of Report3

Device Details

Brand NameADVIA 2120I
Generic NameHEMATOLOGY ANALAYZER, PRODUCT CODE:
Product CodeGKL
Date Received2011-10-26
Model NumberADVIA 2120I
Catalog Number067-A004
Lot NumberN/A
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerSIEMENS HEALTHCARE DIAGNOSTICS
Manufacturer Address511 BENEDICT AVE TARRYTOWN NY 10591 US 10591


Patients

Patient NumberTreatmentOutcomeDate
10 2011-10-26

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