MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2020-02-26 for XXL ESOPHAGEAL 23375 manufactured by Boston Scientific Corporation.
[181181923]
It was reported that balloon rupture occurred. The 90% stenosed target lesion was located in the right common femoral vein. A 18-6/5. 8/75 xxl balloon catheter was advanced for dilatation. However, the balloon ruptured at 2 atmospheres for 3 minutes. Another 16-4/5. 8/75 xxl balloon catheter was selected but at 3 atmospheres for 3 minutes, same thing happened. The device was removed from the patient's body. The procedure was completed with another of the same device. No patient complications were reported.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 2134265-2020-01929 |
MDR Report Key | 9753008 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2020-02-26 |
Date of Report | 2020-02-25 |
Date of Event | 2020-02-05 |
Date Mfgr Received | 2020-02-05 |
Device Manufacturer Date | 2019-07-23 |
Date Added to Maude | 2020-02-26 |
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 | XXL ESOPHAGEAL |
Generic Name | DILATOR, ESOPHAGEAL |
Product Code | KNQ |
Date Received | 2020-02-26 |
Model Number | 23375 |
Catalog Number | 23375 |
Lot Number | 0024153584 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
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 | 2020-02-26 |