JGRLOC B2B RD SS SLD DRL KIT N/A 110007337

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 2020-01-02 for JGRLOC B2B RD SS SLD DRL KIT N/A 110007337 manufactured by Zimmer Biomet, Inc..

MAUDE Entry Details

Report Number0001825034-2019-05813
MDR Report Key9538019
Report SourceDISTRIBUTOR,HEALTH PROFESSION
Date Received2020-01-02
Date of Report2020-01-02
Date of Event2019-12-11
Date Mfgr Received2019-12-12
Device Manufacturer Date2019-03-08
Date Added to Maude2020-01-02
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 SS SLD DRL KIT
Generic NameFASTENER, FIXATION
Product CodeHTN
Date Received2020-01-02
Returned To Mfg2019-12-20
Model NumberN/A
Catalog Number110007337
Lot Number019950
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerZIMMER BIOMET, INC.
Manufacturer Address56 E. BELL DRIVE WARSAW IN 46582 US 46582


Patients

Patient NumberTreatmentOutcomeDate
10 2020-01-02

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