PITUITARY RONGEUR BLACK 3MM LATERAL 8733-7153

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 2018-10-03 for PITUITARY RONGEUR BLACK 3MM LATERAL 8733-7153 manufactured by Zimmer Biomet Spine Inc..

Event Text Entries

[122513564] Udi number: na. Current information is insufficient to permit a valid conclusion about the cause of this event. A follow up report will be sent upon completion of the device evaluation.
Patient Sequence No: 1, Text Type: N, H10


[122513565] It was reported that the tip of a rongeur broke off during surgery. This resulted in a delay longer than 30 minutes in order to retrieve the broken piece from the wound. The procedure was completed using an alternative rongeur. There were no reported patient impacts associated with the delay.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3012447612-2018-00794
MDR Report Key7930650
Report SourceDISTRIBUTOR,HEALTH PROFESSION
Date Received2018-10-03
Date of Report2019-02-06
Date of Event2018-08-31
Date Mfgr Received2019-02-05
Device Manufacturer Date2016-08-18
Date Added to Maude2018-10-03
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 ContactMS. ASHLEY MCPHERSON
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 BLACK 3MM LATERAL
Generic NameRONGEUR
Product CodeHTX
Date Received2018-10-03
Returned To Mfg2018-09-17
Model NumberNA
Catalog Number8733-7153
Lot NumberIM00272
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
101. Other 2018-10-03

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