TIE-IN? 8563003

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,consum report with the FDA on 2019-11-04 for TIE-IN? 8563003 manufactured by Wright Medical Technology, Inc..

Event Text Entries

[170141130] Neither the device nor applicable imaging films were returned to the manufacturer for evaluation, therefore, the cause of the event cannot be determined.
Patient Sequence No: 1, Text Type: N, H10


[170141131] Allegedly, the implant broke in half and the patient underwent a revision surgery.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1043534-2019-00187
MDR Report Key9273387
Report SourceCOMPANY REPRESENTATIVE,CONSUM
Date Received2019-11-04
Date of Report2019-10-11
Date of Event2019-06-18
Date Mfgr Received2019-10-11
Device Manufacturer Date2016-07-08
Date Added to Maude2019-11-04
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 ContactMR MATTHEW PARRISH
Manufacturer Street1023 CHERRY RD
Manufacturer CityMEMPHIS TN 38117
Manufacturer CountryUS
Manufacturer Postal38117
Manufacturer G1WRIGHT MEDICAL TECHNOLOGY, INC.
Manufacturer Street11576 MEMPHIS ARLINGTON RD
Manufacturer CityARLINGTON TN 38002
Manufacturer CountryUS
Manufacturer Postal Code38002
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTIE-IN?
Generic NamePROSTHESIS, WRIST, CARPAL TRAPEZIUM
Product CodeKYI
Date Received2019-11-04
Model Number8563003
Lot Number1580834
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerWRIGHT MEDICAL TECHNOLOGY, INC.
Manufacturer Address11576 MEMPHIS ARLINGTON RD ARLINGTON TN 38002 US 38002


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2019-11-04

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