MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2020-03-31 for COYOTE ES 24701 manufactured by Boston Scientific Corporation.
[185941237]
It was reported that balloon rupture occured. The 100% target lesion was located in the mildly tortuous ang severely calcified common iliac artery. A 2mm x 20mm x 142cm coyote es balloon catheter was advanced for dilatation. However, during first inflation at 3 atmosphere, the balloon ruptured. The procedure was completed with another of same device. No patient complications nor serious injuries were reported.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 2134265-2020-04178 |
MDR Report Key | 9907233 |
Report Source | COMPANY REPRESENTATIVE,FOREIG |
Date Received | 2020-03-31 |
Date of Report | 2020-03-31 |
Date of Event | 2020-03-18 |
Date Mfgr Received | 2020-03-18 |
Device Manufacturer Date | 2019-10-30 |
Date Added to Maude | 2020-03-31 |
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 | TWO SCIMED PLACE |
Manufacturer City | MAPLE GROVE MN 55311 |
Manufacturer Country | US |
Manufacturer Postal Code | 55311 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | COYOTE ES |
Generic Name | CATHETER, ANGIOPLASTY, PERIPHERAL, TRANSLUMINAL |
Product Code | LIT |
Date Received | 2020-03-31 |
Model Number | 24701 |
Catalog Number | 24701 |
Lot Number | 0024680528 |
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 | 2020-03-31 |