MAUDE Adverse Event Report: EKOS CORPORATION EKOSONIC ENDOVASCULAR CATHETER; CATHETER, CONTINUOUS FLUSH

Catalog Number	500-55150
Medical Device Problem Codes	Fracture (1260); Device Inoperable (1663); Device Handling Problem (3265)
Health Effect - Clinical Code	No Known Impact Or Consequence To Patient (2692)
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The catheter (sn: (b)(4)) was returned to ekos on 7/5/2017 for evaluation.The catheter evaluation confirmed the ultrasound core was fractured and the fracture occurred at end of treatment zone next to shaft to treatment zone joint.Examination of the ultrasound core shows indications of a prior kink in the fracture region, and some bending on internal wires.A definitive root cause could not be identified.Ekosonic endovascular device instructions for use states: do not deform or kink the ultrasound core during delivery into the infusion catheter.If the ultrasound core is kinked at any time, do not attempt to use it, as kinking may lead to degraded performance or fracture during use.Review of the manufacturing records indicates that the product was manufactured according to specification following all applicable procedures and the finished device met all acceptance criteria prior to release.
Event or Problem Description
A 106cm/50cm ekosonic catheter (sn: (b)(4)) was used to treat a patient with peripheral arterial occlusion in early (b)(6) 2017, exact event date was not provided.After successfully placed infusion catheter (part of the ekosonic catheter) in the patient, the treating physician tried to place ultrasound core ( microsonic device) and the ultrasound core wire fractured inside the infusion catheter.The physician removed the catheter and placed another ekos device with no further issues.The patient was not harmed and lysed completely after new 50cm device was placed in position.

• Brand Name: EKOSONIC ENDOVASCULAR CATHETER
• Common Device Name: CATHETER, CONTINUOUS FLUSH
• Manufacturer (Section D): EKOS CORPORATION; 11911 north creek parkway s; bothell WA 98011 8809
• MDR Report Key: 6710728
• Report Number: 3001627457-2017-00018
• Device Sequence Number: 2013683
• Product Code: KRA
• UDI-Device Identifier: 00858593006189
• UDI-Public: 00858593006189
• Combination Product (Y/N): N
• Initial Reporter State: WA
• Initial Reporter Country: US
• PMA/510(K) Number: K140151
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: health professional,user faci
• Initial Reporter Occupation: Physician
• Type of Report: Initial
• Report Date (Section B): 06/28/2017

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Physician
• Device Expiration Date: 02/12/2020
• Device Catalogue Number: 500-55150
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 07/05/2017
• Was the Report Sent to FDA?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 06/28/2017
• Initial Report FDA Received Date: 07/13/2017
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1