HARGIS CORONOID CLAMP N/A 01-0145

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-04-05 for HARGIS CORONOID CLAMP N/A 01-0145 manufactured by Biomet Microfixation.

Event Text Entries

[72194644] Without a product return, no product evaluation is able to be conducted. Photographs were provided which confirm the instrument is broken. 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. Device product code gdj.
Patient Sequence No: 1, Text Type: N, H10


[72194645] It was reported the instrument broke during surgery. The broken piece did not fall into the patient and there was no patient injury or delay in surgery as a result of this event. A back-up instrument was available and the surgery was completed successfully.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0001032347-2017-00257
MDR Report Key6459420
Date Received2017-04-05
Date of Report2017-04-03
Date Mfgr Received2017-03-09
Device Manufacturer Date2005-08-04
Date Added to Maude2017-04-05
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 Report0

Device Details

Brand NameHARGIS CORONOID CLAMP
Generic NameCLAMP, MANUAL SURGICAL INSTRUMENT FOR GENERAL USE
Product CodeGDJ
Date Received2017-04-05
Model NumberN/A
Catalog Number01-0145
Lot Number984260
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
10 2017-04-05

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