FEMORAL HEAD STERILE PRODUCT N/A 00801803602

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer report with the FDA on 2019-11-12 for FEMORAL HEAD STERILE PRODUCT N/A 00801803602 manufactured by Zimmer Manufacturing B.v..

MAUDE Entry Details

Report Number0002648920-2019-00811
MDR Report Key9311018
Report SourceCONSUMER
Date Received2019-11-12
Date of Report2019-11-05
Date of Event2019-04-29
Date Mfgr Received2019-06-14
Device Manufacturer Date2014-09-02
Date Added to Maude2019-11-12
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
Generic NamePROSTHESIS, HIP
Product CodeJDL
Date Received2019-11-12
Model NumberN/A
Catalog Number00801803602
Lot Number62813853
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
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. Hospitalization; 2. Required No Informationntervention 2019-11-12

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.