MODULAR CATHCART BALL 48MM OD 1363-48-000 136348000

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 2020-01-02 for MODULAR CATHCART BALL 48MM OD 1363-48-000 136348000 manufactured by Depuy Orthopaedics Inc Us.

Event Text Entries

[174486393] (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


[174486394] It was reported that the patients left hip was revised due to infection and an antibiotic spacer was placed. Doi: (b)(6) 2019. Dor: (b)(6) 2019, left hip.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1818910-2020-00058
MDR Report Key9538308
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2020-01-02
Date of Report2019-12-09
Date of Event2019-12-09
Date Mfgr Received2020-01-30
Device Manufacturer Date2019-06-14
Date Added to Maude2020-01-02
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 ContactMS. KARA DITTY-BOVARD
Manufacturer Street1210 WARD AVENUE
Manufacturer CityWEST CHESTER PA 193800988
Manufacturer CountryUS
Manufacturer Postal193800988
Manufacturer Phone6107428552
Manufacturer G1JJM (SUZHOU) LTD. 3006356043
Manufacturer StreetNO.299 CHANGYANG ST SUZHOU INDUSTRIAL PARK
Manufacturer CitySUZHOU JIANGSU 21512-6
Manufacturer CountryCH
Manufacturer Postal Code21512-6
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameMODULAR CATHCART BALL 48MM OD
Generic NameHEMI HIP IMPLANT : HIP ACETABULAR METAL HEMI
Product CodeLZY
Date Received2020-01-02
Model Number1363-48-000
Catalog Number136348000
Lot NumberD19060100
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerDEPUY ORTHOPAEDICS INC US
Manufacturer Address700 ORTHOPAEDIC DRIVE WARSAW IN 465810988 US 465810988


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2020-01-02

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