RUSCH EQUIPLITE MTL DISP MILL 3 004650003

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06,07 report with the FDA on 2013-08-07 for RUSCH EQUIPLITE MTL DISP MILL 3 004650003 manufactured by Teleflex.

Event Text Entries

[17445889] The event is reported as: the customer alleges that the miller 3 disposable blade will not stay fastened (clicked in) to the handle. No pt injury reported.
Patient Sequence No: 1, Text Type: D, B5


[17744068] The device sample was not returned for evaluation at the time of this report.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1044475-2013-00117
MDR Report Key3284563
Report Source06,07
Date Received2013-08-07
Date of Report2013-07-18
Date of Event2013-07-18
Date Mfgr Received2013-07-18
Date Added to Maude2013-10-31
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 ContactMARGIE BURTON, RN RA
Manufacturer StreetP. O. BOX 12600
Manufacturer CityRESEARCH TRIANGLE PARK NC 27709
Manufacturer CountryUS
Manufacturer Postal27709
Manufacturer Phone9194334965
Manufacturer G1TELEFLEX
Manufacturer Street2917 WECK DR.
Manufacturer CityRESEARCH TRIANGLE PARK NC 27709
Manufacturer CountryUS
Manufacturer Postal Code27709
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameRUSCH EQUIPLITE MTL DISP MILL 3
Generic NameLARYNGOSCOPE BLADE
Product CodeEQN
Date Received2013-08-07
Catalog Number004650003
Lot Number1207832
Device AvailabilityY
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerTELEFLEX
Manufacturer AddressRESEARCH TRIANGLE PARK NC 27709 US 27709


Patients

Patient NumberTreatmentOutcomeDate
10 2013-08-07

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