CHISEL BLADE 10MM 399.55

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 2018-11-05 for CHISEL BLADE 10MM 399.55 manufactured by Wrights Lane Synthes Usa Products Llc.

Event Text Entries

[126166270] Complainant part is expected to be returned for manufacturer review/investigation, but has yet to be received. Initial reporter is synthes sales consultant. Without a lot number the device history records review could not be completed. Product was not returned. Based on the information available, it has been determined that no corrective and/or preventative action is proposed. This complaint will be accounted for and monitored via post market surveillance activities. If additional information is made available, the investigation will be updated as applicable. Device was used for treatment, not diagnosis. 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


[126166271] Device report from synthes (b)(6) reports an event as follows: it was reported that on an unknown date, thirtyeight (38) chisel blades were found in the medical device reprocessing department (mdrd) and tagged as broken. There was no patient or surgical involvement. The thirtyeight (38) devices are addressed in (b)(4). This report is for one (1) 10mm chisel blade. This is report 3 of 10 for (b)(4).
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2939274-2018-54795
MDR Report Key8038887
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2018-11-05
Date of Report2018-10-18
Date Mfgr Received2018-12-18
Device Manufacturer Date2017-07-24
Date Added to Maude2018-11-05
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 ContactMICHAEL COTE
Manufacturer Street1302 WRIGHTS LANE EAST
Manufacturer CityWEST CHESTER PA 19380
Manufacturer CountryUS
Manufacturer Postal19380
Manufacturer Phone6107195000
Manufacturer G1SYNTHES TUTTLINGEN
Manufacturer StreetUNTER HASSLEN 5
Manufacturer CityTUTTLINGEN 78532
Manufacturer CountryGM
Manufacturer Postal Code78532
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCHISEL BLADE 10MM
Generic NameCHISEL,SURGICAL INSTRUMENT
Product CodeFZO
Date Received2018-11-05
Returned To Mfg2018-11-08
Model Number399.55
Catalog Number399.550
Lot NumberT154169
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerWRIGHTS LANE SYNTHES USA PRODUCTS LLC
Manufacturer Address1302 WRIGHTS LANE EAST WEST CHESTER PA 19380 US 19380


Patients

Patient NumberTreatmentOutcomeDate
10 2018-11-05

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