JGRLOC B2B RD TI SLD DRL KIT N/A 110007345

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 2019-04-23 for JGRLOC B2B RD TI SLD DRL KIT N/A 110007345 manufactured by Zimmer Biomet, Inc..

Event Text Entries

[142751410] (b)(4). Customer has indicated that the product will not be returned to zimmer biomet for investigation, discarded. The investigation is in process. Once the investigation has been completed, a follow-up mdr will be submitted. Multiple mdr reports were filed for this event, please see associated reports: 0001825034 - 2019 - 01723.
Patient Sequence No: 1, Text Type: N, H10


[142751411] It was reported that during the surgery two jugger locs were pulled out from the patient bone. No additional information is available for this event.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0001825034-2019-01724
MDR Report Key8539347
Report SourceDISTRIBUTOR,HEALTH PROFESSION
Date Received2019-04-23
Date of Report2019-06-27
Date of Event2019-03-14
Date Mfgr Received2019-06-19
Device Manufacturer Date2018-02-22
Date Added to Maude2019-04-23
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 NameJGRLOC B2B RD TI SLD DRL KIT
Generic NameFASTENER, FIXATION
Product CodeHTN
Date Received2019-04-23
Model NumberN/A
Catalog Number110007345
Lot Number294490
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerZIMMER BIOMET, INC.
Manufacturer Address56 E. BELL DRIVE WARSAW IN 46582 US 46582


Patients

Patient NumberTreatmentOutcomeDate
1110007345 2019-04-23

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