ADVANCED CONTROL I-BASE, DC 5803

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,user f report with the FDA on 2020-02-27 for ADVANCED CONTROL I-BASE, DC 5803 manufactured by Mizuho Orthopedic Systems, Inc..

Event Text Entries

[183889738] It was reported that the table attempted to be moved/tilted in the operating room (or) and the patient almost fell down - status of the patient unknown.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2921578-2020-00010
MDR Report Key9763213
Report SourceCOMPANY REPRESENTATIVE,USER F
Date Received2020-02-27
Date of Report2020-02-27
Date Mfgr Received2020-02-24
Device Manufacturer Date2015-08-31
Date Added to Maude2020-02-27
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationBIOMEDICAL ENGINEER
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactANNE LEBLANC
Manufacturer Street30031 AHERN AVENUE
Manufacturer CityUNION CITY, CA
Manufacturer CountryUS
Manufacturer Phone4291500233
Manufacturer G1MIZUHO ORTHOPEDIC SYSTEMS, INC.
Manufacturer Street30031 AHERN AVENUE
Manufacturer CityUNION CITY, CA
Manufacturer CountryUS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameADVANCED CONTROL I-BASE, DC
Generic NameSURGICAL OPERATING TABLE
Product CodeJEA
Date Received2020-02-27
Model Number5803
Catalog Number5803
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerMIZUHO ORTHOPEDIC SYSTEMS, INC.
Manufacturer Address30031 AHERN AVENUE UNION CITY, CA US


Patients

Patient NumberTreatmentOutcomeDate
10 2020-02-27

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