FEMORAL TEMPLATE STD LM/RL SIZE 1 160141

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,other report with the FDA on 2019-12-23 for FEMORAL TEMPLATE STD LM/RL SIZE 1 160141 manufactured by Mako Surgical Corp..

Event Text Entries

[175876261] As part of the normal complaint follow-up, an evaluation of the event has been initiated by mako surgical. A supplemental report will be submitted when additional information becomes available.
Patient Sequence No: 1, Text Type: N, H10


[175876262] As reported by a mako product manager: "if we are not wrong, we noticed a mistake of translation for the mako restoris size 1 femoral trial ref 160141... In english it? S lm/rl while the translation in french means internal right/external left. "a. Pdf supplied of the label appears to be a sample label, not a packaging label. It is unknown if any physical labels/ devices are involved at this time.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3005985723-2019-00918
MDR Report Key9513167
Report SourceCOMPANY REPRESENTATIVE,OTHER
Date Received2019-12-23
Date of Report2020-03-13
Date of Event2019-11-26
Date Mfgr Received2020-02-14
Date Added to Maude2019-12-23
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 ContactMR. COLLIN NEITZEL
Manufacturer Street325 CORPORATE DRIVE
Manufacturer CityMAHWAH NJ 07430
Manufacturer CountryUS
Manufacturer Postal07430
Manufacturer Phone2018315000
Manufacturer G1MAKO SURGICAL CORP.
Manufacturer Street2555 DAVIE ROAD
Manufacturer CityFORT LAUDERDALE FL 33317
Manufacturer CountryUS
Manufacturer Postal Code33317
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameFEMORAL TEMPLATE STD LM/RL SIZE 1
Generic NamePROSTHESIS, KNEE PATELLOFEMOROTIBIAL, PARTIAL, SEMI-CONSTRAINED, CEMENTED, POLYM
Product CodeNPJ
Date Received2019-12-23
Model Number160141
Catalog Number160141
Lot NumberUNKNOWN
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerMAKO SURGICAL CORP.
Manufacturer Address2555 DAVIE ROAD FORT LAUDERDALE FL 33317 US 33317


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-12-23

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