MAUDE Adverse Event Report: ABBOTT VASCULAR INC. GRAFTMASTER; CORONARY STENT DELIVERY SYSTEM

Model Number	1012580-16
Medical Device Problem Code	Failure to Advance (2524)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	09/17/2024
Type of Reportable Event	Serious Injury
Event or Problem Description
It was reported that a perforation occurred post coronary atherectomy in the mid left anterior descending (lad).A 2.8x16 mm graftmaster covered stent failed to reach the lesion.A 2.8x16 mm graftmaster covered stent was implanted but failed to seal the perforation.A 3.5x16 mm graftmaster covered stent was implanted in the left main to circumflex to jail the lad and sealed the perforation; however, the patient decompensated and cardiopulmonary resuscitation was performed.An effusion was noted on echocardiogram and pericardial drain was performed.The patient coded and was given medication to stabilize blood pressure.The patient was transferred to the icu post procedure.The patient was do not resuscitate and they expired.No additional information was provided.
Additional Manufacturer Narrative
Manufacturer's investigation is still pending at this time.Results and conclusions will be provided in the final report.The additional device referenced in b5 is filed under a separate medwatch report number.
Additional Manufacturer Narrative
The device was not returned for analysis.Production record and corrective and preventative actions (capa) reviews were performed and revealed no indication of a product quality issue.Additionally, a query of the complaint handling database for the reported lot revealed there is no indication of a lot specific issue.Medical review was performed: this was a case to treat a perforation in a mid-left anterior descending artery (mid-lad) in a 63-year-old male patient who presented with an st elevated myocardial infarction (stemi).It was reported that the perforation occurred after an atherectomy in the mid-lad.Due to the information provided, it can not be definitively stated that the 2.8 x 16 graftmaster was the direct contributor or cause of this patient¿s death.It is unknown why the 2.8 x 16 failed to reach the lesion.The patient was experiencing an st elevated myocardial infarction (stemi) at the time of the procedure.The morphology of their coronary arteries is unknown, as is the vessel dominance.The implantation of the 3.5 x 16 graftmaster in the lm and lcx, effectively jailing off the lad artery entirely, is most likely a direct cause of this patient¿s death.However, it is not clear if this is due to a product failure, the patient¿s medical status, or, rather, a medical procedural decision in an attempt to seal the mid-lad perforation.If additional information is received, this medical review will be updated as required.Based on the information provided, a definitive cause for the reported issue could not be determined.Based on the results of the complaint investigation, there is no indication of a product quality issue with respect to the design, manufacture, or labeling of the device.

• Brand Name: GRAFTMASTER
• Common Device Name: CORONARY STENT DELIVERY SYSTEM
• Manufacturer (Section D): ABBOTT VASCULAR INC.; 3200 lakeside drive; santa clara CA 95054 2807
• Manufacturer (Section G): ABBOTT VASCULAR, REG # 3005718570 (P099); cashel road; clonmel tipperary ; EI
• Manufacturer Contact: lindsey bell ; 26531 ynez rd.; temecula, CA 92591-4628 ; 9519143996
• MDR Report Key: 20440650
• Report Number: 2024168-2024-12082
• Device Sequence Number: 7995172
• Product Code: MAF
• UDI-Device Identifier: 08717648176340
• UDI-Public: (01)08717648176340(17)250930(10)3102541
• Combination Product (Y/N): N
• Initial Reporter State: IN
• Initial Reporter Country: US
• PMA/510(K) Number: H000001
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Health Professional,Company Representative
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 10/22/2024

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Expiration Date: 09/30/2025
• Device Model Number: 1012580-16
• Device Catalogue Number: 1012580-16
• Device Lot Number: 3102541
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 09/20/2024
• Supplement Date Received by Manufacturer: 10/17/2024
• Initial Report FDA Received Date: 10/14/2024
• Supplement Report FDA Received Date: 10/22/2024
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 10/25/2023
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other
• Patient Age: 63 YR
• Patient Sex: Male