FEMORAL HEAD STERILE PRODUCT DO NOT RESTERILIZE 12/14 TAPER N/A 00801803603

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer,distributor,health p report with the FDA on 2020-03-30 for FEMORAL HEAD STERILE PRODUCT DO NOT RESTERILIZE 12/14 TAPER N/A 00801803603 manufactured by Zimmer Manufacturing B.v..

MAUDE Entry Details

Report Number0002648920-2020-00211
MDR Report Key9900806
Report SourceCONSUMER,DISTRIBUTOR,HEALTH P
Date Received2020-03-30
Date of Report2020-03-30
Date of Event2011-12-11
Date Mfgr Received2020-03-05
Device Manufacturer Date2011-10-17
Date Added to Maude2020-03-30
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 NameFEMORAL HEAD STERILE PRODUCT DO NOT RESTERILIZE 12/14 TAPER
Generic NamePROSTHESIS, HIP
Product CodeLPH
Date Received2020-03-30
Model NumberN/A
Catalog Number00801803603
Lot Number61907738
OperatorHEALTH PROFESSIONAL
Device Availability*
Device Eval'ed by MfgrR
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. Other 2020-03-30

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