MAUDE Adverse Event Report: BOSTON SCIENTIFIC CORPORATION MUSTANG; CATHETER, BILIARY, DIAGNOSTIC

Model Number	24674
Medical Device Problem Code	Failure to Deflate (4060)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	02/06/2024
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
E1: initial reporter address 1: (b)(6).
Event or Problem Description
It was reported that balloon deflation failure occurred.The target lesion was located in the cephalic vein.An 8.0 x 60, 75cm mustang balloon catheter was advanced for dilation.During the procedure, the balloon was inflated up to 14 atmospheres for 2 minutes.When trying to deflate the balloon, it would not fully deflate.After several minutes of trying and waiting with no success, the physician then used a syringe to manually deflate the balloon.The physician then carefully removed the balloon over the wire with the nurse holding onto the introducer sheath.The balloon was in 10% undeflated state.The procedure was completed with another of the same device.No patient complications were reported.
Additional Manufacturer Narrative
E1: initial reporter address 1: (b)(6) hospital.Device evaluated by mfr.: a mustang 8.0 x 60, 75cm was received for analysis.A visual examination identified that the balloon was not folded which indicates that the balloon was subjected to positive pressure.A longitudinal tear was identified in the balloon material.The tear measured 5mm in length and extended from a position 3mm proximal of the distal markerband to 8mm proximal of the distal markerband.A visual examination observed no damage to the tip of the device.A visual and tactile examination found no kinks or damage to the shaft of the device.Both markerbands were undamaged and present on the shaft of the device.
Event or Problem Description
It was reported that balloon deflation failure occurred.The target lesion was located in the cephalic vein.An 8.0 x 60, 75cm mustang balloon catheter was advanced for dilation.During the procedure, the balloon was inflated up to 14 atmospheres for 2 minutes.When trying to deflate the balloon, it would not fully deflate.After several minutes of trying and waiting with no success, the physician then used a syringe to manually deflate the balloon.The physician then carefully removed the balloon over the wire with the nurse holding onto the introducer sheath.The balloon was in 10% undeflated state.The procedure was completed with another of the same device.No patient complications were reported.

• Brand Name: MUSTANG
• Common Device Name: CATHETER, BILIARY, DIAGNOSTIC
• Manufacturer (Section D): BOSTON SCIENTIFIC CORPORATION; 300 boston scientific way; marlborough MA 01752
• Manufacturer (Section G): BOSTON SCIENTIFIC CORPORATION; pmt 741 persiaran cassia selat; bandarcassia, pulau pinan 14110 ; MY 14110
• Manufacturer Contact: rachel shields ; 4100 hamline ave n; arden hills, MN 55112 ; 6512422111
• MDR Report Key: 19025103
• Report Number: 2124215-2024-19622
• Device Sequence Number: 12589782
• Product Code: FGE
• UDI-Device Identifier: 08714729793885
• UDI-Public: 08714729793885
• Combination Product (Y/N): N
• Initial Reporter Country: SN
• PMA/510(K) Number: K141521
• 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
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 04/29/2024

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: 07/30/2026
• Device Model Number: 24674
• Device Catalogue Number: 24674
• Device Lot Number: 0032115150
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 03/26/2024
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Follow-Up
• Initial Date Received by Manufacturer: 03/08/2024
• Supplement Date Received by Manufacturer: 04/11/2024
• Initial Report FDA Received Date: 04/02/2024
• Supplement Report FDA Received Date: 04/29/2024
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 07/31/2023
• 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
• Patient Sex: Unknown