UNKNOWN ZIMMER TM SHOULDER STEM

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,health profession report with the FDA on 2016-03-07 for UNKNOWN ZIMMER TM SHOULDER STEM manufactured by Zimmer Inc.

Event Text Entries

[39797953] (b)(4). This report will be amended when our investigation is complete.
Patient Sequence No: 1, Text Type: N, H10


[39797954] It was reported a patient was revised due to instability.
Patient Sequence No: 1, Text Type: D, B5


[50416036] No device or photos were received; therefore the condition of the device is unknown. Device history records cannot be reviewed since the part and lot number is unknown. This device is used for treatment. Product history search cannot be completed since the lot number is unknown. No probable cause is determined with the provided information.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1822565-2016-00583
MDR Report Key5483935
Report SourceDISTRIBUTOR,HEALTH PROFESSION
Date Received2016-03-07
Date of Report2016-02-11
Date Mfgr Received2016-07-19
Date Added to Maude2016-03-07
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 ContactKEVIN ESCAPULE
Manufacturer StreetP.O. BOX 708
Manufacturer CityWARSAW IN 465810708
Manufacturer CountryUS
Manufacturer Postal465810708
Manufacturer Phone8006136131
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameUNKNOWN ZIMMER TM SHOULDER STEM
Generic NameSHOULDER PROSTHESIS
Product CodeKWR
Date Received2016-03-07
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerZIMMER INC
Manufacturer AddressP.O. BOX 708 WARSAW IN 465810708 US 465810708


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2016-03-07

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