C-LEG KNEE JOINT 3C98-2=7.1

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 2019-02-06 for C-LEG KNEE JOINT 3C98-2=7.1 manufactured by Otto Bock Healthcare Products Gmbh.

Event Text Entries

[135137127] A soldering defect at the tube adapters strain gauge was detected which led to erroneous sensor signals and caused the occurred event.
Patient Sequence No: 1, Text Type: N, H10


[135137128] Knee moves between free motion and no charge lock or safety mode. Beeps frequently. Could not get knee to connect. Patient lived in (b)(6).
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9615892-2019-00001
MDR Report Key8309450
Report SourceDISTRIBUTOR,HEALTH PROFESSION
Date Received2019-02-06
Date of Report2019-02-06
Date of Event2018-12-10
Date Mfgr Received2019-01-10
Device Manufacturer Date2014-04-02
Date Added to Maude2019-02-06
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR. REINHARD WOLKERSTORFER
Manufacturer StreetBREHMSTRASSE 16
Manufacturer CityVIENNA, 1110
Manufacturer CountryAU
Manufacturer Postal1110
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameC-LEG KNEE JOINT
Generic NameEXTERNAL ABOVE KNEE PROSTHESIS
Product CodeISY
Date Received2019-02-06
Returned To Mfg2018-12-20
Model Number3C98-2=7.1
Catalog Number3C98-2=7.1
OperatorLAY USER/PATIENT
Device AvailabilityR
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerOTTO BOCK HEALTHCARE PRODUCTS GMBH
Manufacturer AddressBREHMSTRASSE 16 VIENNA, 1110 AU 1110


Patients

Patient NumberTreatmentOutcomeDate
10 2019-02-06

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