LEVO ARM 7887-050

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2019-10-28 for LEVO ARM 7887-050 manufactured by Mizuho Orthopedic Systems, Inc..

Event Text Entries

[183886571] It was reported nearing the end of the procedure the levo arm gave out and was completely limp/moveable without pressing either button.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2921578-2019-00038
MDR Report Key9247202
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2019-10-28
Date of Report2019-10-28
Date of Event2019-10-25
Date Mfgr Received2019-10-25
Device Manufacturer Date2018-02-22
Date Added to Maude2019-10-28
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactANNE LEBLANC
Manufacturer Street30031 AHERN AVENUE
Manufacturer CityUNION CITY CA 945871234
Manufacturer CountryUS
Manufacturer Postal945871234
Manufacturer Phone5104291500
Manufacturer G1MIZUHO ORTHOPEDIC SYSTEMS, INC.
Manufacturer Street30031 AHERN AVENUE
Manufacturer CityUNION CITY CA 945871234
Manufacturer CountryUS
Manufacturer Postal Code945871234
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameLEVO ARM
Generic NameHEAD POSITIONING
Product CodeJEA
Date Received2019-10-28
Model Number7887-050
Catalog Number7887-050
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 945871234 US 945871234


Patients

Patient NumberTreatmentOutcomeDate
10 2019-10-28

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