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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: OTTO BOCK HEALTHCARE PRODUCTS GMBH GENIUM X3; EXTERNAL ABOVE KNEE PROSTHESIS

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OTTO BOCK HEALTHCARE PRODUCTS GMBH GENIUM X3; EXTERNAL ABOVE KNEE PROSTHESIS Back to Search Results
Model Number 3B5-2
Device Problem Device Handling Problem (3265)
Patient Problems Fall (1848); Damage to Ligament(s) (1952)
Event Date 04/01/2020
Event Type  Injury  
Manufacturer Narrative
Evaluation and investigation of the device showed no relevant error which may have caused or contributed to the occurred event.
 
Event Description
Wrong joint behavior - sporadically no swing phase release, device blocked when level walking and on stairs.Customer fell while walking down stairs.Noises during swing phase; cracking noises.
 
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Brand Name
GENIUM X3
Type of Device
EXTERNAL ABOVE KNEE PROSTHESIS
Manufacturer (Section D)
OTTO BOCK HEALTHCARE PRODUCTS GMBH
brehmstrasse 16
vienna, vienna 1110
AU  1110
Manufacturer Contact
reinhard wolkerstorfer
brehmstrasse 16
vienna, vienna 1110
AU   1110
MDR Report Key10061489
MDR Text Key191266828
Report Number9615892-2020-00005
Device Sequence Number1
Product Code ISY
Combination Product (y/n)N
Reporter Country CodeGM
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type distributor,health profession
Reporter Occupation Other Health Care Professional
Type of Report Initial
Report Date 04/21/2020
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received05/15/2020
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator Lay User/Patient
Device Model Number3B5-2
Device Catalogue Number3B5-2
Was Device Available for Evaluation? Device Returned to Manufacturer
Date Returned to Manufacturer05/13/2020
Is the Reporter a Health Professional? Yes
Date Manufacturer Received04/21/2020
Was Device Evaluated by Manufacturer? Yes
Date Device Manufactured05/31/2017
Is the Device Single Use? No
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Initial
Patient Sequence Number1
Patient Outcome(s) Hospitalization; Required Intervention;
Patient Age53 YR
Patient Weight108
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