ALTIVATE SHOULDER 521-07-254

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 2019-03-21 for ALTIVATE SHOULDER 521-07-254 manufactured by Encore Medical, L.p..

Event Text Entries

[139530740] Revision surgery - due to the patient dislocating. The surgeon converted the patient to a reverse shoulder system.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1644408-2019-00219
MDR Report Key8441577
Report SourceCOMPANY REPRESENTATIVE
Date Received2019-03-21
Date of Report2019-04-09
Date of Event2019-02-21
Date Mfgr Received2019-03-27
Device Manufacturer Date2018-09-17
Date Added to Maude2019-03-21
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 54, E-PLUS
Product CodePAO
Date Received2019-03-21
Model Number521-07-254
Catalog Number521-07-254
Lot Number894U1051
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerENCORE MEDICAL, L.P.
Manufacturer Address9800 METRIC BLVD. AUSTIN TX 787586313 US 787586313


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2019-03-21

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