MESHGRAFT II INSTRUMENT ONLY 00219500100

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2020-03-02 for MESHGRAFT II INSTRUMENT ONLY 00219500100 manufactured by Zimmer Surgical, Inc..

MAUDE Entry Details

Report Number0001526350-2020-00241
MDR Report Key9775347
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2020-03-02
Date of Report2020-03-02
Date of Event2020-02-07
Date Mfgr Received2020-02-07
Date Added to Maude2020-03-02
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 DRIVE
Manufacturer CityWARSAW IN 46582
Manufacturer CountryUS
Manufacturer Postal46582
Manufacturer Phone5745273773
Manufacturer G1ZIMMER SURGICAL, INC.
Manufacturer Street200 WEST OHIO AVENUE
Manufacturer CityDOVER OH 44622
Manufacturer CountryUS
Manufacturer Postal Code44622
Single Use3
Previous Use Code3
Removal Correction NumberN/A
Event Type3
Type of Report3

Device Details

Brand NameMESHGRAFT II INSTRUMENT ONLY
Generic NameEXPANDER, SURGICAL, SKIN GRAFT
Product CodeFZW
Date Received2020-03-02
Returned To Mfg2020-02-14
Catalog Number00219500100
Lot NumberN/A
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerZIMMER SURGICAL, INC.
Manufacturer Address200 WEST OHIO AVENUE DOVER OH 44622 US 44622


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-02

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