OSTRUM ANTRUM PUNCH BACKBITER RT 1/EA 3712034

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06,user facility report with the FDA on 2014-01-08 for OSTRUM ANTRUM PUNCH BACKBITER RT 1/EA 3712034 manufactured by Medtronic Xomed, Inc..

Event Text Entries

[19925934] It was reported that during a fess procedure, the instrument broke in the patient's nose. A small piece was retrieved from the patient during the procedure and the surgery was successfully completed.
Patient Sequence No: 1, Text Type: D, B5


[20179941] (b)(4). This device is used for therapeutic purposes. Product evaluation: no analysis results available; device has not been returned. Method: no testing methods performed.
Patient Sequence No: 1, Text Type: N, H10


[101909111] If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1045254-2014-00010
MDR Report Key3561081
Report Source06,USER FACILITY
Date Received2014-01-08
Date of Report2013-12-18
Date of Event2013-12-16
Date Mfgr Received2013-12-18
Device Manufacturer Date2013-03-01
Date Added to Maude2014-04-09
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 Location3
Manufacturer ContactMICHELLE ALFORD
Manufacturer Street6743 SOUTHPOINT DRIVE NORTH
Manufacturer CityJACKSONVILLE FL 32216
Manufacturer CountryUS
Manufacturer Postal32216
Manufacturer Phone9043328197
Manufacturer G1MEDTRONIC XOMED, INC.
Manufacturer Street6743 SOUTHPOINT DRIVE NORTH
Manufacturer CityJACKSONVILLE FL 32216
Manufacturer CountryUS
Manufacturer Postal Code32216
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameOSTRUM ANTRUM PUNCH BACKBITER RT 1/EA
Generic NamePUNCH, NASAL
Product CodeKAY
Date Received2014-01-08
Model Number3712034
Catalog Number3712034
Lot Number13031
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerMEDTRONIC XOMED, INC.
Manufacturer Address6743 SOUTHPOINT DRIVE NORTH JACKSONVILLE FL 32216 US 32216


Patients

Patient NumberTreatmentOutcomeDate
10 2014-01-08

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