UNKNOWN COMPREHENSIVE REVERSE HUMERAL TRAY N/A

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2018-10-18 for UNKNOWN COMPREHENSIVE REVERSE HUMERAL TRAY N/A manufactured by Zimmer Biomet, Inc..

Event Text Entries

[124129806] (b)(4). Udi # n/a. Foreign country: (b)(4). Customer has indicated that the product is in process of being returned to zimmer biomet for investigation. Once the investigation has been completed, a follow-up mdr will be submitted.
Patient Sequence No: 1, Text Type: N, H10


[124129807] It has been reported that patient had an initial reverse total shoulder arthroplasty. Subsequently patient was revised due to humeral tray fracture. Patient was reported to have had a fall which may have contributed to the fracture. No additional patient consequences were reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0001825034-2018-09816
MDR Report Key7978691
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2018-10-18
Date of Report2018-12-21
Date of Event2018-09-19
Date Mfgr Received2018-11-29
Date Added to Maude2018-10-18
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 ContactMS. CHRISTINA ARNT
Manufacturer Street56 E. BELL DR.
Manufacturer CityWARSAW IN 46582
Manufacturer CountryUS
Manufacturer Postal46582
Manufacturer Phone5745273773
Manufacturer G1ZIMMER BIOMET, INC.
Manufacturer Street56 E. BELL DRIVE
Manufacturer CityWARSAW IN 46582
Manufacturer CountryUS
Manufacturer Postal Code46582
Single Use3
Previous Use Code3
Removal Correction NumberN/A
Event Type3
Type of Report3

Device Details

Brand NameUNKNOWN COMPREHENSIVE REVERSE HUMERAL TRAY
Generic NamePROSTHESIS, SHOULDER
Product CodeMJT
Date Received2018-10-18
Model NumberN/A
Catalog NumberNI
Lot NumberNI
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerZIMMER BIOMET, INC.
Manufacturer Address56 E. BELL DRIVE WARSAW IN 46582 US 46582


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Required No Informationntervention 2018-10-18

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