MAUDE Adverse Event Report: MICROVENTION, INC. WEB SL; INTRASACCULAR DEVICES

Model Number W5-4-3-MVI-3

Device Problems Device Dislodged or Dislocated (2923); Separation Problem (4043)

Patient Problem No Clinical Signs, Symptoms or Conditions (4582)

Event Date 03/06/2023

Event Type  Injury  

Manufacturer Narrative

A search for non-conformances associated with this part/lot number combination did not reveal any production-related issues relevant to the complaint that occurred during manufacturing of the device.The device was implanted in the patient and not returned to the manufacturer for analysis.Imaging was provided and its analysis is currently ongoing.

Event Description

It was reported that a web device was implanted in a left ica aneurysm but would not detach after the use of the detachment controller.The microcatheter was used to push the implant off of the delivery pusher, but the implant dislodged from the aneurysm.A stent was used to tack the protruding web against the arterial wall.The patient was reported to have woke up from anesthesia neurologically intact.

Manufacturer Narrative

Six (6) angiographic images are supplied.They are all blurry and of poor quality.They are not labeled as to side, date or time.Two problems are described in this report (one in each ica).Image 1: poor quality ica oblique roadmap with very little contrast material.A medium sized aneurysm is seen, possibly in the pcom area.A microcatheter with only a few mm of unopened web is seen at the neck of the aneurysm.Image 2: single shot unsubtracted lateral radiograph centered on skull base, no contrast.A well opened pipeline flow diverter spans from the high supraclinoid ica/proximal m1 to just below the ophthalmic segment.A web is seen adjacent to the pipeline, off the posterior wall of the supraclinoid ica.Image 3: different, ap-ish projection, of the same as xavier bad web 2.A web with a lot of skull bone is superimposed.The image is not interpretable.Image 4: same as xavier bad web 2, but with some small amount of contrast injected.Image 5: single shot unsubtracted ap radiograph centered on skull base; contrast seen in left ica circulation.A web is seen end-on in the proximal 1/3 of the supraclinoid ica, as both distal and proximal markers are almost superimposed.Image 6: single shot unsubtracted lateral radiograph centered on skull base, no contrast.A second well opened pipeline is seen spanning from the high supraclinoid ica to just below the ophthalmic segment.Posterior to it is a second web device.The previously described contralateral web and pipeline are also seen on this image.The complication described is not explained by these images.Without the return and physical evaluation of the device, the investigation cannot determine if a condition exists that would have caused on contributed to the reported event.

Event Description

See h.10.

• Brand Name: WEB SL
• Type of Device: INTRASACCULAR DEVICES
• Manufacturer (Section D): MICROVENTION, INC.; 35 enterprise; aliso viejo CA 92656
• Manufacturer Contact: terrence callahan ; 35 enterprise; aliso viejo, CA 92656 ; 7142478000
• MDR Report Key: 16632748
• MDR Text Key: 312195126
• Report Number: 2032493-2023-00635
• Device Sequence Number: 1
• Product Code: OPR
• UDI-Device Identifier: 00842429110829
• UDI-Public: (01)00842429110829(11)220112(17)241231(10)0000140480
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: P170032
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Health Professional,User Facility,Company Representative
• Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date: 03/06/2023

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 03/28/2023
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Model Number: W5-4-3-MVI-3
• Device Catalogue Number: W5-4-3
• Device Lot Number: 0000140480
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: No
• Date Manufacturer Received: 04/24/2023
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Date Device Manufactured: 01/12/2022
• Is the Device Single Use?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Initial
• Patient Sequence Number: 1
• Patient Outcome(s): Required Intervention
• Patient Sex: Female