ASR ACETABULAR IMPLANT 70 999806370

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer,foreign,other report with the FDA on 2020-03-17 for ASR ACETABULAR IMPLANT 70 999806370 manufactured by Depuy International Ltd - 8010379.

MAUDE Entry Details

Report Number1818910-2020-08223
MDR Report Key9842226
Report SourceCONSUMER,FOREIGN,OTHER
Date Received2020-03-17
Date of Report2020-02-28
Date of Event2018-07-18
Date Mfgr Received2020-03-26
Device Manufacturer Date2004-10-28
Date Added to Maude2020-03-17
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 ContactKARA DITTY-BOVARD
Manufacturer Street700 ORTHOPEDICS DRIVE
Manufacturer CityWARSAW IN 465810988
Manufacturer CountryUS
Manufacturer Postal465810988
Manufacturer Phone6107428552
Manufacturer G1DEPUY INTERNATIONAL LTD - 8010379
Manufacturer StreetST ANTHONYS ROAD
Manufacturer CityLEEDS LS118DT
Manufacturer CountryUK
Manufacturer Postal CodeLS11 8DT
Single Use3
Remedial ActionRC
Previous Use Code3
Removal Correction NumberZ-1749/1816-2011
Event Type3
Type of Report3

Device Details

Brand NameASR ACETABULAR IMPLANT 70
Generic NameASR HIP SYSTEM : HIP METAL ACETABULAR CUPS
Product CodeKXA
Date Received2020-03-17
Catalog Number999806370
Lot Number1800637
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
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 2020-03-17

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