TOTAL HIP BALL 32MM +11 1014-70-000 101470000

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2020-03-31 for TOTAL HIP BALL 32MM +11 1014-70-000 101470000 manufactured by Depuy International Ltd - 8010379.

Event Text Entries

[186723510] (b)(4). If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
Patient Sequence No: 1, Text Type: N, H10


[186723511] It was reported that the surgeon revised a duraloc constrained liner that had dislocated. The liner and head were removed and new implants used. There was no noted deficiency with the explanted items. Doi: unknown. Dor: (b)(6) 2020, right hip.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1818910-2020-09751
MDR Report Key9904330
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2020-03-31
Date of Report2020-03-12
Date of Event2020-03-12
Date Mfgr Received2020-03-12
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
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactKARA DITTY-BOVARD
Manufacturer Street700 ORTHOPAEDIC DR.
Manufacturer CityWARSAW IN 465810988
Manufacturer CountryUS
Manufacturer Postal465810988
Manufacturer Phone6107428552
Manufacturer G1DEPUY INT'L LTD. 8010379
Manufacturer StreetST ANTHONYS ROAD
Manufacturer CityLEEDS LS118 DT
Manufacturer CountryUK
Manufacturer Postal CodeLS11 8 DT
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTOTAL HIP BALL 32MM +11
Generic NameLARGE TAPER FEMORAL HEADS : HIP METAL FEMORAL HEADS
Product CodeJDI
Date Received2020-03-31
Model Number1014-70-000
Catalog Number101470000
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerDEPUY INTERNATIONAL LTD - 8010379
Manufacturer AddressST. ANTHONY'S ROAD LEEDS LS118DT UK LS11 8DT


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2020-03-31

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