G7 HI-WALL E1 LINER 32MM C N/A 010000925

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,foreign report with the FDA on 2019-11-19 for G7 HI-WALL E1 LINER 32MM C N/A 010000925 manufactured by Zimmer Biomet, Inc..

MAUDE Entry Details

Report Number0001825034-2019-05257
MDR Report Key9340539
Report SourceDISTRIBUTOR,FOREIGN
Date Received2019-11-19
Date of Report2019-11-19
Date of Event2019-10-30
Date Mfgr Received2019-11-11
Device Manufacturer Date2019-07-04
Date Added to Maude2019-11-19
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 NameG7 HI-WALL E1 LINER 32MM C
Generic NamePROSTHESIS, HIP
Product CodePBI
Date Received2019-11-19
Model NumberN/A
Catalog Number010000925
Lot Number6569795
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
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
10 2019-11-19

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