JOHNSON & JOHNSON M SERIES 85-3635

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2011-01-24 for JOHNSON & JOHNSON M SERIES 85-3635 manufactured by .

Event Text Entries

[1902706] Painful left total hip with a loose femoral component - cemented stem. Same pt as (b)(4).
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report NumberMW5019144
MDR Report Key1972754
Date Received2011-01-24
Date of Report2011-01-24
Date of Event2002-02-23
Date Added to Maude2011-02-02
Event Key0
Report Source CodeVoluntary report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Single Use0
Previous Use Code0
Event Type3
Type of Report3

Device Sequence Number: 1

Brand NameJOHNSON & JOHNSON
Generic NameCEMENTED FEMORAL COMPONENT
Product CodeJDI
Date Received2011-01-24
Catalog NumberM SERIES 85-3635
Lot Number1006598
Device AvailabilityN
Device Sequence No1
Device Event Key0

Device Sequence Number: 2

Brand NameDEPUY
Generic NameFEMORAL CEMENT RESTRICTOR
Product CodeJDK
Date Received2011-01-24
Catalog Number5460-14-000
Lot NumberW1XA21092
Device AvailabilityN
Device Sequence No2
Device Event Key0
ManufacturerDEPUY ORTHOPAEDICS, INC.
Manufacturer AddressWARSAW IN 46581 US 46581

Device Sequence Number: 3

Brand NameENDURANCE BONE CEMENT
Generic NameCEMENTED FEMORAL COMPONENT
Product CodeLOD
Date Received2011-01-24
Catalog Number5450 50 000
Lot NumberV4SAA4000
Device Expiration Date2004-11-30
Device AvailabilityN
Device Sequence No3
Device Event Key0
ManufacturerDEPUY ORTHOPAEDICS, INC.
Manufacturer AddressWARSAW IN 46581 US 46581


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Deathisabilit 2011-01-24

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