MAUDE Adverse Event Report: STRYKER NEUROVASCULAR CORK TARGET XL 360 SOFT 14MM X 50CM; DEVICE, NEUROVASCULAR EMBOLIZATION

Model Number	M0036121450
Medical Device Problem Code	Premature Separation (4045)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	04/21/2021
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Report 3 of 3.
Event or Problem Description
It was reported that during a procedure in the left anterior communicating artery, the physician successfully catheterized the aneurysm with a micro catheter.The guide wire was retracted and the first coil was loaded into the micro catheter, but after advancing approximately one or two thirds in the microcatheter shaft, it got stuck in the micro catheter.When the physician tried to pull back the first coil, it detached in the micro catheter and both devices were removed and replaced with similar devices.The same event happened with the second coil and micro catheter and the physician removed and replaced them with a third subject coil and micro catheter which also had the same event happen.This caused a 30 minute surgical delay.The physician removed the third subject coil and micro catheter and replaced with similar devices to complete the procedure without any clinical consequences to the patient.
Event or Problem Description
It was reported that during a procedure in the left anterior communicating artery, the physician successfully catheterized the aneurysm with a micro catheter.The guide wire was retracted and the first coil was loaded into the micro catheter, but after advancing approximately one or two thirds in the microcatheter shaft, it got stuck in the micro catheter.When the physician tried to pull back the first coil, it detached in the micro catheter and both devices were removed and replaced with similar devices.The same event happened with the second coil and micro catheter and the physician removed and replaced them with a third subject coil and micro catheter which also had the same event happen.This caused a 30 minute surgical delay.The physician removed the third subject coil and micro catheter and replaced with similar devices to complete the procedure without any clinical consequences to the patient.
Additional Manufacturer Narrative
H4 manufacturing date ¿ added.H3 device evaluated by mfg ¿updated.H3 summary attached - updated.D4 expiration date - added.Due to the automated mes system, there are controls in the manufacturing process to ensure the product met specifications upon release.On initial inspection, the device was returned within the sl-10.The lot number was confirmed with the packaging returned with the device.On visual & microscope inspection, the main coil was protruding from the concurrent sl-10 catheter.The proximal contact wire was intact.The coil delivery wire was kinked/bent.The main coil was retracted from the catheter shaft.The distal tip was found to be intact.A large quantity of blood exited the catheter shaft.The main coil was stretched.The suture was damaged.On functional testing, the main coil was jammed in the catheter shaft and had to be retracted to remove the coil.The reported event is covered in the device directions for use (dfu).As well, the risk of the reported event is documented in the risk documentation and there are current controls to mitigate the risk of the as reported event.The damage noted to the device would be indicative of the as reported defect.It was seen that the main coil was jammed in the concurrent sl-10 catheter.It was found to be badly stretched but remained attached.The delivery wire was also seen to be kinked/bent.Additional information provided by the customer indicated that the device was confirmed to be in good condition during preparation/prior to use on the patient, preparation/set-up was performed as per the dfu and continuous flush was maintained for the duration of the procedure.Therefore, the as reported 'coil jammed' can be confirmed.The as reported/analyzed 'coil jammed' as well as the analyzed 'main coil stretched' and 'main coil suture damage' will be assigned procedural factors as these defects appear to be associated with a product that met stryker and design and manufacturing specifications and was used in accordance with the dfu, but performance was limited due to procedural or anatomical factors during use.The as reported 'main coil prematurely detached during use' will not be confirmed as the coil was found to be attached.An assignable cause of not confirmed will be assigned to the as reported 'main coil prematurely detached during use'.The as analyzed 'coil delivery wire kinked bent' will be assigned handling damage as the issue is due to handling of the product or portion of the product during the clinical procedure, upon removal of the product from the packaging, or preparation of the product prior to use.The manufacturer has reviewed all information and determined this event no longer meets the requirement of the reportable event for the device in question.

• Brand Name: TARGET XL 360 SOFT 14MM X 50CM
• Common Device Name: DEVICE, NEUROVASCULAR EMBOLIZATION
• Manufacturer (Section D): STRYKER NEUROVASCULAR CORK; ida industrial estate; model farm road; cork NA ; EI NA
• MDR Report Key: 11830556
• Report Number: 3008881809-2021-00207
• Device Sequence Number: 16355147
• Product Code: HCG
• UDI-Device Identifier: 04546540711540
• UDI-Public: 04546540711540
• Combination Product (Y/N): N
• Initial Reporter State: FL
• Initial Reporter Country: US
• PMA/510(K) Number: K153658
• 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): 08/13/2021

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: 05/06/2022
• Device Model Number: M0036121450
• Device Catalogue Number: M0036121450
• Device Lot Number: 21414017
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 05/07/2021
• Initial Date Received by Manufacturer: 04/21/2021
• Supplement Date Received by Manufacturer: 07/20/2021
• Initial Report FDA Received Date: 05/17/2021
• Supplement Report FDA Received Date: 08/13/2021
• 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: EXCELSIOR SL-10 (MICRO CATHETER).; EXCELSIOR SL-10 (MICRO CATHETER).
• Patient Age: 65 YR