PITUITARY RONGEUR ? STRAIGHT ? 4MM 2856-14

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor report with the FDA on 2018-06-27 for PITUITARY RONGEUR ? STRAIGHT ? 4MM 2856-14 manufactured by Zimmer Biomet Spine Inc..

Event Text Entries

[112559631] 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


[112559632] It was reported that the jaw on a rongeur was found to have broken after it went through post-operative cleaning. There were no patient impacts.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3012447612-2018-00529
MDR Report Key7643019
Report SourceDISTRIBUTOR
Date Received2018-06-27
Date of Report2018-10-26
Date of Event2018-05-29
Date Mfgr Received2018-10-23
Device Manufacturer Date2006-12-15
Date Added to Maude2018-06-27
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 ContactMR. GEOFFREY GANNON
Manufacturer Street10225 WESTMOOR DR. NA
Manufacturer CityWESTMINSTER CO 80021
Manufacturer CountryUS
Manufacturer Postal80021
Manufacturer Phone3034437500
Manufacturer G1ZIMMER BIOMET SPINE INC.
Manufacturer Street10225 WESTMOOR DR. NA
Manufacturer CityWESTMINSTER CO 80021
Manufacturer CountryUS
Manufacturer Postal Code80021
Single Use3
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NamePITUITARY RONGEUR ? STRAIGHT ? 4MM
Generic NameRONGEUR
Product CodeHTX
Date Received2018-06-27
Returned To Mfg2018-06-28
Model NumberNA
Catalog Number2856-14
Lot Number42DG
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerZIMMER BIOMET SPINE INC.
Manufacturer Address10225 WESTMOOR DR. NA WESTMINSTER CO 80021 US 80021


Patients

Patient NumberTreatmentOutcomeDate
10 2018-06-27

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