MAUDE Adverse Event Report: BOSTON SCIENTIFIC CORPORATION COYOTE; CATHETER, ANGIOPLASTY, PERIPHERAL, TRANSLUMINAL

Model Number	24699
Medical Device Problem Code	Material Rupture (1546)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	10/17/2024
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that balloon rupture occurred.Vascular access was obtained via ipsilateral antegrade approach.The 99% stenosed target lesion was located in the moderately tortuous and moderately calcified right posterior tibial artery.A non-boston scientific sheath, microcatheter and guidewire were advanced and placed, and the inflation was performed using a 1.5x40 coyote balloon catheter.Subsequently, this 2.5mm x 220mm x 150cm coyote balloon catheter was used and inflated; however, it ruptured at 12 atmospheres during the third inflation for 30 seconds.The device was removed without any problems.The balloon was replaced with a 2.5x150 coyote balloon and the inflation was continued followed by an additional dilation at the distal side with another 2x40 coyote balloon.The procedure was completed, and no complications were reported.The patient was in good condition after the procedure.

• Brand Name: COYOTE
• Common Device Name: CATHETER, ANGIOPLASTY, PERIPHERAL, TRANSLUMINAL
• Manufacturer (Section D): BOSTON SCIENTIFIC CORPORATION; 300 boston scientific way; marlborough MA 01752
• Manufacturer (Section G): BOSTON SCIENTIFIC CORPORATION; two scimed place; maple grove MN 55311
• Manufacturer Contact: rachel shields ; 4100 hamline ave n; arden hills, MN 55112 ; 6512422111
• MDR Report Key: 20584852
• Report Number: 2124215-2024-68618
• Device Sequence Number: 12892078
• Product Code: DQY
• UDI-Device Identifier: 08714729796893
• UDI-Public: 08714729796893
• Combination Product (Y/N): N
• Initial Reporter Country: JA
• PMA/510(K) Number: K111295
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Other,Foreign,Health Professional,Company Representative,Distributor
• Initial Reporter Occupation: Physician
• Type of Report: Initial
• Report Date (Section B): 10/31/2024

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: 01/16/2026
• Device Model Number: 24699
• Device Catalogue Number: 24699
• Device Lot Number: 0030863983
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 10/17/2024
• Initial Report FDA Received Date: 10/31/2024
• Date Device Manufactured: 01/17/2023
• 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
• Concomitant Medical Products and Therapy/Usage Dates: GUIDEWIRE: GLADIUS, ASTATO 9-12, 9-40; INFLATION DEVICE: NIPRO; INTRODUCER SHEATH: 5FR DESTINATION
• Patient Sex: Unknown