EXODONTIA ELEVATOR #46R, SERRATED N/A 09-0252

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2019-04-26 for EXODONTIA ELEVATOR #46R, SERRATED N/A 09-0252 manufactured by Biomet Microfixation.

Event Text Entries

[145276742] (b)(4). Product has been received by zimmer biomet and the investigation is in process. Once the investigation has been completed, a follow-up mdr will be submitted.
Patient Sequence No: 1, Text Type: N, H10


[145276743] It was reported that the instrument fractured at the tip during a tooth extraction. The fractured piece was suctioned from the patients mouth. No adverse events have been reported as a result of the malfunction.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0001032347-2019-00254
MDR Report Key8558265
Report SourceHEALTH PROFESSIONAL
Date Received2019-04-26
Date of Report2019-05-31
Date of Event2019-03-26
Date Mfgr Received2019-05-06
Device Manufacturer Date2018-01-05
Date Added to Maude2019-04-26
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationDENTIST
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMRS. MERRIANNE CASSIDY
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 NameEXODONTIA ELEVATOR #46R, SERRATED
Generic NameELEVATOR, SURGICAL, DENTAL
Product CodeEMJ
Date Received2019-04-26
Returned To Mfg2019-04-26
Model NumberN/A
Catalog Number09-0252
Lot Number121217K17
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerBIOMET MICROFIXATION
Manufacturer Address1520 TRADEPORT DRIVE JACKSONVILLE FL 32218 US 32218


Patients

Patient NumberTreatmentOutcomeDate
10 2019-04-26

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