THIN OSTEOTOME HANDLE 242210000

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2019-04-30 for THIN OSTEOTOME HANDLE 242210000 manufactured by Depuy Orthopaedics, Inc. 1818910.

Event Text Entries

[143568947] Product complaint : (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


[143568948] It was reported that the screw to fasten chisel was broken when the surgeon struck the osteotome handle reversely with the hammer during the revision surgery on (b)(6) 2019. The broken fragment was retrieved and confirmed there was no remaining in the patient's body. The surgery was completed with extra osteotome handle and there was no surgical delay. There was no adverse consequence to the patient.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1818910-2019-92025
MDR Report Key8565335
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2019-04-30
Date of Report2019-04-09
Date of Event2019-04-09
Date Mfgr Received2019-07-01
Device Manufacturer Date2008-07-15
Date Added to Maude2019-04-30
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. KARA DITTY-BOVARD
Manufacturer Street1210 WARD AVENUE
Manufacturer CityWEST CHESTER PA 193800988
Manufacturer CountryUS
Manufacturer Postal193800988
Manufacturer Phone6103142063
Manufacturer G1DEPUY ORTHOPAEDICS, INC. 1818910
Manufacturer Street700 ORTHOPAEDIC DRIVE
Manufacturer CityWARSAW IN 465820988
Manufacturer CountryUS
Manufacturer Postal Code465820988
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTHIN OSTEOTOME HANDLE
Generic NameHIP INSTRUMENTS : HANDLES
Product CodeHWM
Date Received2019-04-30
Returned To Mfg2019-05-21
Catalog Number242210000
Lot NumberCS7K54000
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerDEPUY ORTHOPAEDICS, INC. 1818910
Manufacturer Address700 ORTHOPAEDIC DRIVE WARSAW IN 465820988 US 465820988


Patients

Patient NumberTreatmentOutcomeDate
10 2019-04-30

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