MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,distri report with the FDA on 2020-03-30 for MUSTANG 24674 manufactured by Boston Scientific Corporation.
[185665197]
(b)(6).
Patient Sequence No: 1, Text Type: N, H10
[185665198]
It was reported that balloon rupture occurred. The 99% stenosed target lesion was located in a shunt in the moderately tortuous and moderately calcified vessel. A 6. 0 x 20mm, 40cm mustang balloon catheter was used for dilation; however, during inflation the balloon ruptured. The procedure was completed with another of the same device and no patient complications were reported.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 2134265-2020-04053 |
MDR Report Key | 9897945 |
Report Source | COMPANY REPRESENTATIVE,DISTRI |
Date Received | 2020-03-30 |
Date of Report | 2020-03-30 |
Date of Event | 2019-12-31 |
Date Mfgr Received | 2020-03-11 |
Device Manufacturer Date | 2019-10-11 |
Date Added to Maude | 2020-03-30 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | JAY JOHNSON |
Manufacturer Street | TWO SCIMED PLACE |
Manufacturer City | MAPLE GROVE MN 55311 |
Manufacturer Country | US |
Manufacturer Postal | 55311 |
Manufacturer Phone | 7634942574 |
Manufacturer G1 | BOSTON SCIENTIFIC CORPORATION |
Manufacturer Street | BALLYBRIT BUSINESS PARK |
Manufacturer City | GALWAY |
Manufacturer Country | EI |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | MUSTANG |
Generic Name | CATHETER, BILIARY, DIAGNOSTIC |
Product Code | FGE |
Date Received | 2020-03-30 |
Returned To Mfg | 2020-03-25 |
Model Number | 24674 |
Catalog Number | 24674 |
Lot Number | 0024581015 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | BOSTON SCIENTIFIC CORPORATION |
Manufacturer Address | TWO SCIMED PLACE MAPLE GROVE MN 55311 US 55311 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-30 |