COMP PRIMARY STEM 12MM STD N/A 113652

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,distri report with the FDA on 2019-01-15 for COMP PRIMARY STEM 12MM STD N/A 113652 manufactured by Zimmer Biomet, Inc..

Event Text Entries

[133183360] (b)(4). Product has been received by zimmer biomet and the investigation is in process. Once the investigation has been completed, a follow-up mdr will be submitted.
Patient Sequence No: 1, Text Type: N, H10


[133183361] It was reported that during the initial reverse total shoulder arthroplasty, the implant sat 1 mm proud during implantation, following broaching. A new, smaller implant of the next lowest size was used to completed the procedure. A delay of thirty five (35) minutes was noted. No additional patient consequences were noted. No additional information is available at this time.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0001825034-2019-00044
MDR Report Key8251128
Report SourceCOMPANY REPRESENTATIVE,DISTRI
Date Received2019-01-15
Date of Report2019-04-23
Date of Event2018-12-21
Date Mfgr Received2019-04-22
Device Manufacturer Date2017-11-30
Date Added to Maude2019-01-15
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 NameCOMP PRIMARY STEM 12MM STD
Generic NamePROSTHESIS, SHOULDER
Product CodeMBF
Date Received2019-01-15
Returned To Mfg2018-12-26
Model NumberN/A
Catalog Number113652
Lot Number899030
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
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 2019-01-15

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