INTERNAL SCREWDRIVER * 119840

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 08 report with the FDA on 2006-03-03 for INTERNAL SCREWDRIVER * 119840 manufactured by Newdeal S.a..

Event Text Entries

[18910868] During a surery for a 14 year old pt while in final adjustment on the first kalix implant, the distal flat portion of screwdriver snapped off in the implant. The dr could not retrieve from the implant. The dr closed it over anyway with soft tissue and did the second bilateral implant with another instrument. No pt injury was reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9615741-2006-00006
MDR Report Key682288
Report Source08
Date Received2006-03-03
Date of Report2006-03-02
Date Mfgr Received2006-02-03
Date Added to Maude2006-03-09
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 Location0
Manufacturer ContactYANPING WANG
Manufacturer Street311C ENTERPRISE DR
Manufacturer CityPLAINSBORO NJ 08536
Manufacturer CountryUS
Manufacturer Postal08536
Manufacturer Phone6099362322
Manufacturer G1NEWDEAL S.A.
Manufacturer Street10, PLACE D'HELVETIE
Manufacturer CityLYON 69006
Manufacturer CountryFR
Manufacturer Postal Code69006
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameINTERNAL SCREWDRIVER
Generic NameKALIX ASSOCIATED INSTRUMENTS
Product CodeKXX
Date Received2006-03-03
Model Number*
Catalog Number119840
Lot Number*
ID Number*
Device AvailabilityN
Device Eval'ed by MfgrR
Implant FlagN
Date Removed*
Device Sequence No1
Device Event Key671556
ManufacturerNEWDEAL S.A.
Manufacturer Address* LYON FR
Baseline Brand NameINTERNAL SCREWDRIVER
Baseline Generic NameKALIX IMPLANT ASSOCIATED INSTRUMENTS
Baseline Model No*
Baseline Catalog No119840
Baseline ID*


Patients

Patient NumberTreatmentOutcomeDate
10 2006-03-03

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