UNKNOWN SHOULDER HUMERAL STEMS UNK SHOULDER HUMERAL STEM

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2018-06-18 for UNKNOWN SHOULDER HUMERAL STEMS UNK SHOULDER HUMERAL STEM manufactured by Depuy Orthopaedics Inc Us.

Event Text Entries

[111399539] If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
Patient Sequence No: 1, Text Type: N, H10


[111399540] Patient was revised to address pain. Doi: (b)(6) 2012; dor: (b)(6) 2018; right shoulder.
Patient Sequence No: 1, Text Type: D, B5


[117453288] Product complaint # :(b)(4). Investigation summary : no device associated with this report was received for examination. If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1818910-2018-62483
MDR Report Key7611514
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2018-06-18
Date of Report2018-05-23
Date of Event2018-05-23
Date Mfgr Received2018-07-17
Date Added to Maude2018-06-18
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 ContactMR. CHAD GIBSON
Manufacturer Street700 ORTHOPAEDIC DRIVE
Manufacturer CityWARSAW IN 465820988
Manufacturer CountryUS
Manufacturer Postal465820988
Manufacturer Phone5743725905
Manufacturer G1DEPUY ORTHOPAEDICS, INC. 1818910
Manufacturer Street700 ORTHOPAEDIC DRIVE
Manufacturer CityWARSAW IN 465820988
Manufacturer CountryUS
Manufacturer Postal Code465820988
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameUNKNOWN SHOULDER HUMERAL STEMS
Generic NameSHOULDER HUMERAL STEMS
Product CodeMJT
Date Received2018-06-18
Catalog NumberUNK SHOULDER HUMERAL STEM
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerDEPUY ORTHOPAEDICS INC US
Manufacturer Address700 ORTHOPAEDIC DRIVE WARSAW IN 465820988 US 465820988


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2018-06-18

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