I-STAT G3+ CARTRIDGE 03P78-50

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 2020-01-17 for I-STAT G3+ CARTRIDGE 03P78-50 manufactured by Abbott Point Of Care.

MAUDE Entry Details

Report Number2245578-2020-00016
MDR Report Key9601805
Report SourceHEALTH PROFESSIONAL
Date Received2020-01-17
Date of Report2020-01-17
Date of Event2019-01-08
Date Mfgr Received2020-01-08
Date Added to Maude2020-01-17
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 ContactLINDA MACZUSZENKO
Manufacturer Street400 COLLEGE ROAD
Manufacturer CityPRINCETON NJ 085403629
Manufacturer CountryUS
Manufacturer Postal085403629
Manufacturer Phone6136885949
Manufacturer G1ABBOTT POINT OF CARE CANADA LTD.
Manufacturer Street185 CORKSTOWN ROAD
Manufacturer CityK2H 8V4
Manufacturer CountryCA
Manufacturer Postal CodeK2H 8V4
Single Use3
Remedial ActionRC
Previous Use Code3
Removal Correction NumberAPOC2020-002
Event Type3
Type of Report3

Device Details

Brand NameI-STAT G3+ CARTRIDGE
Generic NameG3+ CARTRIDGE
Product CodeCHL
Date Received2020-01-17
Model NumberNA
Catalog Number03P78-50
Lot NumberNA
Device Availability*
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerABBOTT POINT OF CARE
Manufacturer Address400 COLLEGE ROAD PRINCETON NJ 085406607 US 085406607


Patients

Patient NumberTreatmentOutcomeDate
10 2020-01-17

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