ALTIVATE SHOULDER 521-07-246

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 2018-08-10 for ALTIVATE SHOULDER 521-07-246 manufactured by Encore Medical L.p..

Event Text Entries

[116801780] Revision surgery - due to dislocation with leveraging of the glenoid. Dislodgement of the glenoid into the back of the shoulder.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1644408-2018-00759
MDR Report Key7773996
Report SourceCOMPANY REPRESENTATIVE
Date Received2018-08-10
Date of Report2018-08-27
Date of Event2018-08-01
Date Mfgr Received2018-08-27
Device Manufacturer Date2017-07-08
Date Added to Maude2018-08-10
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 ContactTEFFANY HUTTO
Manufacturer Street9800 METRIC BLVD
Manufacturer CityAUSTIN TX 787585445
Manufacturer CountryUS
Manufacturer Postal787585445
Manufacturer G1ENCORE MEDICAL L.P.
Manufacturer Street9800 METRIC BLVD
Manufacturer CityAUSTIN TX 787585445
Manufacturer CountryUS
Manufacturer Postal Code787585445
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameALTIVATE SHOULDER
Generic NameALTIVATE ANATOMIC, ALL-POLY PEGGED GLENOID, SIZE 46, E-PLUS
Product CodePAO
Date Received2018-08-10
Model Number521-07-246
Catalog Number521-07-246
Lot Number892U1022
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerENCORE MEDICAL L.P.
Manufacturer Address9800 METRIC BLVD AUSTIN TX 787585445 US 787585445


Patients

Patient NumberTreatmentOutcomeDate
15201. Required No Informationntervention 2018-08-10

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