MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,user faci report with the FDA on 2016-02-29 for CELLO BALLOON GUIDE CATHETER 1610580 manufactured by Micro Therapeutics, Inc. Dba Ev3 Neurovascular.
[39249177]
The device will not be returned for analysis as it was discarded; therefore the complaint could not be determined. Same event as reported in mdr mfr# 2029214-2016-00121.
Patient Sequence No: 1, Text Type: N, H10
[39249178]
Medtronic received information that during a mechanical thrombectomy procedure in the internal carotid artery (ica), the cello balloon burst and leaked upon inflation. No patient injury as a result of this event. No further information was provided.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 2029214-2016-00120 |
MDR Report Key | 5466928 |
Report Source | HEALTH PROFESSIONAL,USER FACI |
Date Received | 2016-02-29 |
Date of Report | 2016-02-03 |
Date of Event | 2016-01-27 |
Date Mfgr Received | 2016-02-03 |
Device Manufacturer Date | 2015-11-17 |
Date Added to Maude | 2016-02-29 |
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 | TRICHA MILES |
Manufacturer Street | 9775 TOLEDO WAY |
Manufacturer City | IRVINE CA 92618 |
Manufacturer Country | US |
Manufacturer Postal | 92618 |
Manufacturer Phone | 9498373700 |
Manufacturer G1 | MICRO THERAPEUTICS, INC. DBA EV3 NEUROVA |
Manufacturer Street | 9775 TOLEDO WAY |
Manufacturer City | IRVINE CA 92618 |
Manufacturer Country | US |
Manufacturer Postal Code | 92618 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | CELLO BALLOON GUIDE CATHETER |
Generic Name | CATHETER, NEURO-VASCULATURE, OCCLUDING BALLON |
Product Code | NUF |
Date Received | 2016-02-29 |
Model Number | 1610580 |
Lot Number | 5500195 |
Device Expiration Date | 2018-10-01 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | MICRO THERAPEUTICS, INC. DBA EV3 NEUROVASCULAR |
Manufacturer Address | 9775 TOLEDO WAY IRVINE CA 92618 US 92618 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2016-02-29 |