CUSHING RONGEUR STRAIGHT 2 MM X 10 MM 00336000000

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign report with the FDA on 2019-05-07 for CUSHING RONGEUR STRAIGHT 2 MM X 10 MM 00336000000 manufactured by Zimmer Biomet, Inc..

Event Text Entries

[144386490] (b)(4). Customer has indicated that the product will not be returned to zimmer biomet for investigation, as the device was discarded by hospital. The investigation is in process. Once the investigation has been completed, a follow-up mdr will be submitted. Product not received.
Patient Sequence No: 1, Text Type: N, H10


[144386491] It was reported that the patient underwent lumbar discectomy and while removing the loose disc fragments, the instrument broke. Surgery was prolonged by an hour. The patient retained broken rongeur jaw piece. No additional patient consequences were reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0001822565-2019-01899
MDR Report Key8588604
Report SourceFOREIGN
Date Received2019-05-07
Date of Report2019-06-19
Date of Event2019-02-15
Date Mfgr Received2019-06-19
Device Manufacturer Date2008-01-16
Date Added to Maude2019-05-07
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. CHRISTINA ARNT
Manufacturer Street56 E. BELL DR.
Manufacturer CityWARSAW IN 46582
Manufacturer CountryUS
Manufacturer Postal46582
Manufacturer Phone5745273773
Manufacturer G1ZIMMER BIOMET, INC.
Manufacturer Street56 E. BELL DRIVE
Manufacturer CityWARSAW IN 46582
Manufacturer CountryUS
Manufacturer Postal Code46582
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameCUSHING RONGEUR STRAIGHT 2 MM X 10 MM
Generic NameTRAUMA INSTRUMENTATION
Product CodeHTX
Date Received2019-05-07
Catalog Number00336000000
Lot Number60858642
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerZIMMER BIOMET, INC.
Manufacturer Address56 E. BELL DRIVE WARSAW IN 46582 US 46582


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Required No Informationntervention 2019-05-07

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