EQUINOXE UNK

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 2020-03-20 for EQUINOXE UNK manufactured by Exactech, Inc..

Event Text Entries

[189055939] Pending evaluation.
Patient Sequence No: 1, Text Type: N, H10


[189055940] As reported, the elderly and skinny male patient had failure of a reverse total shoulder due to dislocation in 2017. The initial implant date is unknown. This patient has a history of falling and dislocating his shoulder. All available information has been provided at this time.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1038671-2020-00251
MDR Report Key9860929
Report SourceCOMPANY REPRESENTATIVE
Date Received2020-03-20
Date of Report2020-03-20
Date of Event2017-01-01
Date Mfgr Received2020-02-28
Date Added to Maude2020-03-20
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 ContactKATE JACOBSON
Manufacturer Phone3523771140
Manufacturer G1EXACTECH, INC.
Manufacturer Street2320 NW 66 CT
Manufacturer CityGAINESVILLE FL 32653
Manufacturer CountryUS
Manufacturer Postal Code32653
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameEQUINOXE
Generic NameLINER
Product CodeKWT
Date Received2020-03-20
Catalog NumberUNK
Lot NumberUNK
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerEXACTECH, INC.
Manufacturer Address2320 NW 66 COURT GAINESVILLE FL 32653 US 32653


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Required No Informationntervention 2020-03-20

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.