MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2019-04-18 for FG GATEWAY OTW JP 1.50MM X 9MM M0032072009150 manufactured by Boston Scientific - Minn.
[142396705]
Subject device is not available.
Patient Sequence No: 1, Text Type: N, H10
[142396706]
It was reported that the patient underwent angioplasty with the subject balloon catheter. A non-severe vessel dissection occurred at the right internal carotid artery (ica). A stent was placed to treat the dissection. The procedure was completed without problems. There were no clinical consequences to the patient..
Patient Sequence No: 1, Text Type: D, B5
Report Number | 3008853977-2019-00035 |
MDR Report Key | 8528703 |
Report Source | HEALTH PROFESSIONAL |
Date Received | 2019-04-18 |
Date of Report | 2019-06-11 |
Date of Event | 2019-04-10 |
Date Mfgr Received | 2019-05-30 |
Device Manufacturer Date | 2018-10-20 |
Date Added to Maude | 2019-04-18 |
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 | MR. TARA LOPEZ |
Manufacturer Street | 47900 BAYSIDE PARKWAY |
Manufacturer City | FREMONT CA 94538 |
Manufacturer Country | US |
Manufacturer Postal | 94538 |
Manufacturer Phone | 5104132500 |
Manufacturer G1 | BOSTON SCIENTIFIC - MINN |
Manufacturer Street | ONE 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 | FG GATEWAY OTW JP 1.50MM X 9MM |
Generic Name | CATHETER, BALLOON TYPE |
Product Code | GBA |
Date Received | 2019-04-18 |
Catalog Number | M0032072009150 |
Lot Number | 22807391 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | BOSTON SCIENTIFIC - MINN |
Manufacturer Address | ONE SCIMED PLACE MAPLE GROVE MN 55311 US 55311 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other; 2. Required No Informationntervention | 2019-04-18 |