DATEX-OHMEDA S/5 COMPACT AIRWAY MODULE E-CAIO

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06 report with the FDA on 2010-08-04 for DATEX-OHMEDA S/5 COMPACT AIRWAY MODULE E-CAIO manufactured by Ge Healthcare Finland, Oy.

Event Text Entries

[1631383] A customer reported that a unit was failing a leak test. There is an indication in the complaint record that a death or serious injury may have occurred, however, no additional details are known at this time. Ge healthcare's investigation into the reported occurrence is still ongoing. A follow-up report will be issued when the investigation had been completed.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9610105-2010-00013
MDR Report Key1790246
Report Source06
Date Received2010-08-04
Date of Report2010-08-04
Date of Event2010-07-05
Date Mfgr Received2010-07-05
Date Added to Maude2010-08-13
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional0
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactDEBRA LAHR
Manufacturer Street540 W NORTHWEST HWY
Manufacturer CityBARRINGTON IL 600103076
Manufacturer CountryUS
Manufacturer Postal600103076
Manufacturer Phone8472774472
Manufacturer G1GE HEALTHCARE FINLAND, OY
Manufacturer CityHELSINKI
Manufacturer CountryFI
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameDATEX-OHMEDA S/5 COMPACT AIRWAY MODULE E-CAIO
Product CodeCCL
Date Received2010-08-04
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerGE HEALTHCARE FINLAND, OY
Manufacturer AddressHELSINKI FI


Patients

Patient NumberTreatmentOutcomeDate
101. Death 2010-08-04

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