TRANSVERSE DRILL GUIDE 0234500202

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2009-11-03 for TRANSVERSE DRILL GUIDE 0234500202 manufactured by Stryker Endoscopy San Jose.

Event Text Entries

[21287958] It was reported that the doctor was not able to pierce femur while drilling with the subject drill. As doctor also stated, the drill has drilled to a guide. According to the doctor the event took place during surgery. According to doctor the adverse consequence for the pt was linked to the extension of surgery time, as it took 1 hr 30 mins for before doctor managed to drill femur manually without using above mentioned guide. Doctor reported that the tools were crooked.
Patient Sequence No: 1, Text Type: D, B5


[21342283] Add'l info will be provided, once investigation is completed.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2936485-2009-00247
MDR Report Key1522777
Report Source05
Date Received2009-11-03
Date of Report2009-10-05
Date of Event2009-09-09
Date Mfgr Received2009-10-05
Date Added to Maude2009-11-10
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 FDA0
Event Location0
Manufacturer ContactNILA PATEL
Manufacturer Street5900 OPTICAL CT.
Manufacturer CitySAN JOSE CA 95138
Manufacturer CountryUS
Manufacturer Postal95138
Manufacturer Phone4087542000
Manufacturer G1STRYKER ENDOSCOPY SAN JOSE
Manufacturer Street5900 OPTICAL CT.
Manufacturer CitySAN JOSE CA 95138
Manufacturer CountryUS
Manufacturer Postal Code95138
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTRANSVERSE DRILL GUIDE
Generic NameGUIDE
Product CodeLXI
Date Received2009-11-03
Catalog Number0234500202
Lot Number128164
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSTRYKER ENDOSCOPY SAN JOSE
Manufacturer AddressSAN JOSE CA 95138 US 95138


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2009-11-03

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