2G 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 2017-04-25 for 2G OTOMIMIX N/A 7014-3266 manufactured by Biomet Microfixation.

Event Text Entries

[73573782] The instructions for use (ifu) contains mixing instructions. 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


[73573783] It was reported the cement was tested prior to inserting the cement in the patient's ear and it was not hardening. Additional information was requested, however, it was reported no additional information is available.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0001032347-2017-00298
MDR Report Key6518039
Report SourceDISTRIBUTOR,HEALTH PROFESSION
Date Received2017-04-25
Date of Report2017-04-24
Date Mfgr Received2017-03-27
Device Manufacturer Date2016-04-01
Date Added to Maude2017-04-25
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 Name2G OTOMIMIX
Generic NameCEMENT, EAR, NOSE AND THROAT
Product CodeNEA
Date Received2017-04-25
Model NumberN/A
Catalog Number7014-3266
Lot Number824850
ID NumberN/A
Device Expiration Date2018-04-01
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
10 2017-04-25

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