OTOMIMIX N/A 7014-3266

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,health profession report with the FDA on 2017-04-24 for OTOMIMIX N/A 7014-3266 manufactured by Biomet Microfixation.

Event Text Entries

[73491851] Without a product return, no product evaluation is able to be conducted. Current information is insufficient to permit a valid conclusion about the cause of this event. If additional information is obtained that adds value to the relevant content of this report and/or a conclusion can be drawn, a follow-up report will be sent.
Patient Sequence No: 1, Text Type: N, H10


[73491852] It was reported the surgeon was performing a right tympanoplasty procedure. Two packages of otomimix would not solidify during prep. The surgeon explained that the mixture does not harden on the tissue it just falls apart, but the mixture will harden if not in contact with patient's tissue. The surgery was prolonged by an hour due to trying two boxes and then having to go to the third to finish the procedure. There was no negative outcome to the patient.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0001032347-2017-00297
MDR Report Key6515354
Report SourceDISTRIBUTOR,HEALTH PROFESSION
Date Received2017-04-24
Date of Report2017-04-21
Date Mfgr Received2017-03-27
Date Added to Maude2017-04-24
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 ContactMRS. MICHELLE COLE
Manufacturer Street1520 TRADEPORT DRIVE
Manufacturer CityJACKSONVILLE FL 32218
Manufacturer CountryUS
Manufacturer Postal32218
Manufacturer Phone9047414400
Manufacturer G1BIOMET MICROFIXATION
Manufacturer Street1520 TRADEPORT DRIVE
Manufacturer CityJACKSONVILLE FL 32218
Manufacturer CountryUS
Manufacturer Postal Code32218
Single Use3
Previous Use Code3
Removal Correction NumberN/A
Event Type3
Type of Report3

Device Details

Brand NameOTOMIMIX
Generic NameCEMENT, EAR, NOSE AND THROAT
Product CodeNEA
Date Received2017-04-24
Model NumberN/A
Catalog Number7014-3266
Lot Number273310
ID NumberN/A
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBIOMET MICROFIXATION
Manufacturer Address1520 TRADEPORT DRIVE JACKSONVILLE FL 32218 US 32218


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2017-04-24

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