SHORT V OSTEO 7MM X 7 3/4 IN 242109000

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 2019-04-30 for SHORT V OSTEO 7MM X 7 3/4 IN 242109000 manufactured by Depuy Orthopaedics, Inc. 1818910.

Event Text Entries

[143608776] 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


[143608957] It was reported that the tip of instrument sheared off during surgery and needs replacement. All pieces were retrieved from the patient and there was no delay. This is a new instrument and the surgeon feels the product was defective considering it broke in first surgery it was used.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1818910-2019-92061
MDR Report Key8566570
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2019-04-30
Date of Report2019-04-09
Date of Event2019-04-09
Date Mfgr Received2019-06-03
Device Manufacturer Date2019-04-19
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
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 19380XXXX
Manufacturer CountryUS
Manufacturer Postal19380XXXX
Manufacturer Phone6107428552
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 NameSHORT V OSTEO 7MM X 7 3/4 IN
Generic NameKNEE INSTRUMENT : CUTTING INSTRUMENTS
Product CodeHWM
Date Received2019-04-30
Returned To Mfg2019-04-22
Catalog Number242109000
Lot NumberSO2040394
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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