MAUDE Adverse Event Report: STRYKER NEUROVASCULAR-CALIF AXS VECTA 071 ASPIRATION CATHETER (132CM); CATHETER, THROMBUS RETRIEVER

Catalog Number	INC-11129-132
Medical Device Problem Code	Break (1069)
Health Effect - Clinical Code	No Consequences Or Impact To Patient (2199)
Date of Event	06/11/2019
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The subject device is unavailable to manufacturer.
Event or Problem Description
It was reported that during procedure, the subject device was fractured from the proximal to the hub.There were no clinical consequences to the patient due to the reported event.
Additional Manufacturer Narrative
A review of the device history record confirmed that the device met all material, assembly and performance specifications.During analysis, the catheter found to be kinked from its proximal and separated under its strain relief.The shaft at the separated site was severely stretched.Based on visual inspection, the catheter appeared to have been kinked first and then stretched and separated due to excessive manipulation during use.Functional evaluation could not be performed due to the anomalies found on the catheter.Additional information provided by the customer indicated that the device was prepared as per the device directions for use (dfu),no resistance was encountered during the procedure, and a neuro max catheter (non-stryker device) was also used in the procedure.As a result, a probable cause of handling damage has been assigned to the reported event and analyzed anomalies.
Event or Problem Description
It was reported that during procedure, the subject device was fractured from the proximal to the hub.There were no clinical consequence es to the patient due to the reported event.

• Brand Name: AXS VECTA 071 ASPIRATION CATHETER (132CM)
• Common Device Name: CATHETER, THROMBUS RETRIEVER
• Manufacturer (Section D): STRYKER NEUROVASCULAR-CALIF; 47900 bayside parkway; fremont CA 94538
• MDR Report Key: 8724484
• Report Number: 3008853977-2019-00051
• Device Sequence Number: 2472402
• Product Code: NRY
• UDI-Device Identifier: 07613327459234
• UDI-Public: 07613327459234
• Combination Product (Y/N): N
• Initial Reporter State: AZ
• Initial Reporter Country: US
• PMA/510(K) Number: K172167
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: health professional
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 08/13/2019

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: Health Professional
• Device Expiration Date: 08/31/2021
• Device Catalogue Number: INC-11129-132
• Device Lot Number: 13321-01
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 06/24/2019
• Initial Date Received by Manufacturer: 06/11/2019
• Supplement Date Received by Manufacturer: 08/09/2019
• Initial Report FDA Received Date: 06/21/2019
• Supplement Report FDA Received Date: 08/15/2019
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: NEURO MAX MICROCATHETER (NON STRYKER)