CARESTATION 620

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,foreign,health pr report with the FDA on 2020-03-30 for CARESTATION 620 manufactured by Ge Medical Systems (china) Co., Ltd (wuxi).

Event Text Entries

[186175467] The distributor performed a checkout of the system and confirmed the reported issue. The transient board was replaced to resolve the reported issue. No report of patient involvement. The initial reporter is located outside the u. S. , and therefore this information is not provided due to country privacy laws.
Patient Sequence No: 1, Text Type: N, H10


[186175468] The hospital reported an error preventing mechanical ventilation. There was no report of patient involvement.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9710602-2020-00115
MDR Report Key9899894
Report SourceDISTRIBUTOR,FOREIGN,HEALTH PR
Date Received2020-03-30
Date of Report2020-03-30
Date of Event2020-03-04
Date Mfgr Received2020-03-04
Device Manufacturer Date2015-09-11
Date Added to Maude2020-03-30
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 FDA0
Report to FDA3
Event Location3
Manufacturer ContactJOHN SZALINSKI
Manufacturer Street3000 N GRANDVIEW BLVD.
Manufacturer CityWAUKESHA WI
Manufacturer CountryUS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCARESTATION 620
Generic NameANESTHESIA GAS MACHINE
Product CodeBSZ
Date Received2020-03-30
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerGE MEDICAL SYSTEMS (CHINA) CO., LTD (WUXI)
Manufacturer AddressNO. 19 CHANGJIANG ROAD NATIONAL HI-TECH DEV. ZONE WUXI 214028 CH 214028


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-30

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