MAUDE Adverse Event Report: BOSTON SCIENTIFIC CORPORATION STERLING; CATHETER, PERCUTANEOUS

Model Number	24700
Medical Device Problem Code	Material Rupture (1546)
Health Effect - Clinical Code	No Consequences Or Impact To Patient (2199)
Date of Event	04/01/2020
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that balloon rupture occurred.The target lesion was located in the calcified popliteal artery.A 5.0mmx80mmx135cm sterling balloon catheter was advanced for dilatation; however, during the initial inflation at rated burst pressure, the balloon ruptured.The procedure was completed with another of the same device.No patient complications were reported and the patient's status was good.
Additional Manufacturer Narrative
Device evaluation by mfr.: returned product consisted of a sterling balloon catheter.The shaft, hypotube, tip and balloon were microscopically and visually examined.There was a longitudinal tear 41mm long starting from the distal end of the balloon.Inspection of the remainder of the device presented no other damage or irregularities.
Event or Problem Description
It was reported that balloon rupture occurred.The target lesion was located in the calcified popliteal artery.A 5.0mmx80mmx135cm sterling balloon catheter was advanced for dilatation; however, during the initial inflation at rated burst pressure, the balloon ruptured.The procedure was completed with another of the same device.No patient complications were reported and the patient's status was good.

• Brand Name: STERLING
• Common Device Name: CATHETER, PERCUTANEOUS
• Manufacturer (Section D): BOSTON SCIENTIFIC CORPORATION; two scimed place; maple grove MN 55311
• MDR Report Key: 9992135
• Report Number: 2134265-2020-05534
• Device Sequence Number: 3836672
• Product Code: DQY
• UDI-Device Identifier: 08714729122951
• UDI-Public: 08714729122951
• Combination Product (Y/N): N
• Initial Reporter Country: KS
• PMA/510(K) Number: K053116
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: company representative,foreig
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 07/03/2020

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: 06/20/2022
• Device Model Number: 24700
• Device Catalogue Number: 24700
• Device Lot Number: 0023989130
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 06/02/2020
• Initial Date Received by Manufacturer: 04/21/2020
• Supplement Date Received by Manufacturer: 06/30/2020
• Initial Report FDA Received Date: 04/23/2020
• Supplement Report FDA Received Date: 07/03/2020
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Patient Age: 79 YR