TRIOS

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2020-01-15 for TRIOS manufactured by Mizuho Orthopedic Systems, Inc..

Event Text Entries

[183881839] It has been reported there have been "multiple" events where patients have received pressure injuries from their new operating table pads. Specifically, the surgeons and the operating room manager have complained that the pads are too hard and are resulting in patient pressure injuries. No details on the number of patients or the extent of any patient's injuries.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2921578-2020-00001
MDR Report Key9591848
Report SourceCOMPANY REPRESENTATIVE
Date Received2020-01-15
Date of Report2020-01-15
Date Mfgr Received2019-12-31
Date Added to Maude2020-01-15
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
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 NameTRIOS
Generic NamePADS
Product CodeJEA
Date Received2020-01-15
OperatorHEALTH PROFESSIONAL
Device Availability*
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerMIZUHO ORTHOPEDIC SYSTEMS, INC.
Manufacturer Address30031 AHERN AVENUE UNION CITY CA 945871234 US 945871234


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2020-01-15

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