G8 021560

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2019-04-25 for G8 021560 manufactured by Tosoh Corporation.

Event Text Entries

[145947749] The field service engineer (fse) evaluated the g8 analyzer at the customer's site. The fse replaced degasser modules, but the issue did not resolve. The analyzer was replaced.
Patient Sequence No: 1, Text Type: N, H10


[145947750] This report summarizes 1 malfunction event on the g8 analyzer. The review of the event indicated that the g8 analyzer experienced a pressure error message, which caused delayed reporting of critical patient test results. This report was received from one source. There was no indication of patient intervention or adverse health consequences due to the delayed reporting in patient results. . This event did not necessitate remedial action to prevent an unreasonable risk of substantial harm to the public health.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number8031673-2019-00072
MDR Report Key8553041
Report SourceHEALTH PROFESSIONAL
Date Received2019-04-25
Date of Report2019-04-25
Date Added to Maude2019-04-25
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 ContactMS. DORIA ESQUIVEL
Manufacturer StreetSHIBA-KOEN FIRST BUILDING 3-8-2 SHIBA
Manufacturer CityMINATO-KU, TOKYO 1058623
Manufacturer CountryJA
Manufacturer Postal1058623
Manufacturer G1TOSOH CORPORATION
Manufacturer StreetSHIBA-KOEN FIRST BUILDING 3-8-2 SHIBA
Manufacturer CityMINATO-KU, TOKYO 1058623
Manufacturer CountryJA
Manufacturer Postal Code1058623
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameG8
Generic NameG8
Product CodeLCP
Date Received2019-04-25
Model NumberG8
Catalog Number021560
Device AvailabilityY
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerTOSOH CORPORATION
Manufacturer AddressSHIBA-KOEN FIRST BUILDING 3-8-2 SHIBA MINATO-KU, TOKYO 105-8623 JA 105-8623


Patients

Patient NumberTreatmentOutcomeDate
10 2019-04-25

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.