ION NITRIDED BLADE 0940023000

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06 report with the FDA on 2013-11-12 for ION NITRIDED BLADE 0940023000 manufactured by Stryker Instruments-kalamazoo.

Event Text Entries

[4233052] It was reported that the blade cracked in half when tightened during a procedure. The case was completed successfully. There was no medical treatment or intervention required and no adverse consequences associated with this event.
Patient Sequence No: 1, Text Type: D, B5


[11596595] Device was returned and evaluation performed.
Patient Sequence No: 1, Text Type: N, H10


[17570717] It was reported that the blade cracked in half when tightened during a procedure. The case was completed successfully. There was no medical treatment or intervention required and no adverse consequences associated with this event.
Patient Sequence No: 1, Text Type: D, B5


[17777313] Device not yet received for evaluation.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number0001811755-2013-02826
MDR Report Key3465207
Report Source06
Date Received2013-11-12
Date of Report2013-10-24
Date of Event2013-10-22
Date Mfgr Received2014-03-25
Device Manufacturer Date2012-03-27
Date Added to Maude2013-11-12
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 ContactMR. DERVILLIA MURPHY
Manufacturer StreetINSTRUMENTS DIVISION CARRIGTWOHILL BUS. & TECH PARK
Manufacturer CityCARRIGTWOHILL NA
Manufacturer PostalNA
Manufacturer Phone214532900
Manufacturer G1STRYKER INSTRUMENTS-IRELAND
Manufacturer StreetINSTRUMENTS DIVISION CARRIGTWOHILL BUS. & TECH PARK
Manufacturer CityCARRIGTWOHILL MI 49001NA
Manufacturer Postal Code49001 NA
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameION NITRIDED BLADE
Generic NameINSTRUMENT, CAST REMOVAL, AC-POWERED
Product CodeLGH
Date Received2013-11-12
Returned To Mfg2013-11-26
Catalog Number0940023000
Lot Number120870178S
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerSTRYKER INSTRUMENTS-KALAMAZOO
Manufacturer Address4100 EAST MILHAM AVENUE KALAMAZOO MI 49001 US 49001


Patients

Patient NumberTreatmentOutcomeDate
10 2013-11-12

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.