MAUDE Adverse Event Report: OTTO BOCK HEALTHCARE PRODUCTS GMBH GENIUM - BIONIC PROSTHETIC SYSTEM; EXTERNAL ABOVE KNEE PROSTHESIS

Model Number 3B1

Device Problem Device Operates Differently Than Expected (2913)

Patient Problem Concussion (2192)

Event Type  Injury  

Manufacturer Narrative

Device evaluation in progress; supplemental report will be submitted after additional information has been obtained.

Event Description

Patient fell with the motorcycle.No malfunction of the knee joint.The foot or the knee pops (undefined noises) and this should be checked.The user has crashed on a racetrack with the motorcycle, the fall was not caused by the joint, according to mr.(b)(6).

Manufacturer Narrative

According to the event description the patient had a motorcycle accident on a racetrack.Evaluation and investigation of the knee joint showed no relevant error which may have caused or contributed to the occurred event.

• Brand Name: GENIUM - BIONIC PROSTHETIC SYSTEM
• 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 ; 1 5233786
• MDR Report Key: 7062551
• MDR Text Key: 93031629
• Report Number: 9615892-2017-00032
• Device Sequence Number: 1
• Product Code: ISY
• Combination Product (y/n): N
• Reporter Country Code: AU
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: distributor,health profession
• Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date: 12/21/2017

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 11/28/2017
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Lay User/Patient
• Device Model Number: 3B1
• Device Catalogue Number: 3B1
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 11/23/2017
• Is the Reporter a Health Professional?: Yes
• Date Manufacturer Received: 12/06/2017
• Was Device Evaluated by Manufacturer?: Yes
• Date Device Manufactured: 09/18/2013
• Is the Device Single Use?: No
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Initial
• Patient Sequence Number: 1
• Patient Outcome(s): Hospitalization