VERSYS FEMORAL STEM CEMENTED NI 00785001300

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,foreign,health pr report with the FDA on 2020-03-31 for VERSYS FEMORAL STEM CEMENTED NI 00785001300 manufactured by Zimmer Manufacturing B.v..

MAUDE Entry Details

Report Number0002648920-2019-00724
MDR Report Key9902575
Report SourceDISTRIBUTOR,FOREIGN,HEALTH PR
Date Received2020-03-31
Date of Report2020-03-30
Date of Event2019-09-12
Date Mfgr Received2019-09-13
Device Manufacturer Date2010-11-08
Date Added to Maude2020-03-31
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 MANUFACTURING B.V.
Manufacturer StreetTURPEAUX INDUSTRIAL PARK ROUTE #1 KM 123.4 BLDG #1
Manufacturer CityMERCEDITA PR 00715
Manufacturer CountryUS
Manufacturer Postal Code00715
Single Use3
Previous Use Code3
Removal Correction NumberN/A
Event Type3
Type of Report3

Device Details

Brand NameVERSYS FEMORAL STEM CEMENTED
Generic NamePROSTESIS, HIP
Product CodeJDI
Date Received2020-03-31
Returned To Mfg2019-10-16
Model NumberNI
Catalog Number00785001300
Lot Number61651798
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerZIMMER MANUFACTURING B.V.
Manufacturer AddressTURPEAUX INDUSTRIAL PARK ROUTE #1 KM 123.4 BLDG #1 MERCEDITA PR 00715 US 00715


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Required No Informationntervention 2020-03-31

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