CABLE CUTTER 1.8 MM MAXIMUM CABLE DIAMETER N/A 00392501100

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-05-06 for CABLE CUTTER 1.8 MM MAXIMUM CABLE DIAMETER N/A 00392501100 manufactured by Zimmer Biomet, Inc..

Event Text Entries

[144399577] (b)(4). (b)(6). 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


[144399578] It was reported that cutter does not cut the cable. No additional information available.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0001822565-2019-01774
MDR Report Key8583034
Date Received2019-05-06
Date of Report2019-10-08
Date Mfgr Received2019-10-03
Date Added to Maude2019-05-06
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
Removal Correction NumberN/A
Event Type3
Type of Report3

Device Details

Brand NameCABLE CUTTER 1.8 MM MAXIMUM CABLE DIAMETER
Generic NameCUTTER, WIRE
Product CodeHXZ
Date Received2019-05-06
Model NumberN/A
Catalog Number00392501100
Lot NumberUNK
OperatorHEALTH PROFESSIONAL
Device Availability*
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
10 2019-05-06

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