MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 04,05,06 report with the FDA on 2011-10-12 for HYPERGLIDE OCCLUSION BALLOON SYSTEM 104-4112 manufactured by Ev3 Neurovascular.
[2502675]
It was reported the balloon could not be inflated during procedure. It was reported that the balloon was tested for inflation/deflation during preparation and it had worked as intended. No pt injury reported.
Patient Sequence No: 1, Text Type: D, B5
[9572861]
The balloon catheter was returned for evaluation with the guidewire stuck inside the catheter. The guidewire was found broken into two segments inside the catheter. Analysis of the cross section at the break point could not determined the cause of the guidewire failure. (b)(4).
Patient Sequence No: 1, Text Type: N, H10
| Report Number | 2029214-2011-00332 |
| MDR Report Key | 2371407 |
| Report Source | 04,05,06 |
| Date Received | 2011-10-12 |
| Date of Report | 2011-09-30 |
| Date of Event | 2011-08-22 |
| Date Mfgr Received | 2011-09-30 |
| Device Manufacturer Date | 2010-01-25 |
| Date Added to Maude | 2012-03-13 |
| 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 | 0 |
| Event Location | 0 |
| Manufacturer Contact | KIM SALCEDA |
| Manufacturer Street | 9775 TOLEDO WAY |
| Manufacturer City | IRVINE CA 92618 |
| Manufacturer Country | US |
| Manufacturer Postal | 92618 |
| Manufacturer Phone | 9498373700 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | HYPERGLIDE OCCLUSION BALLOON SYSTEM |
| Generic Name | OCCLUSION BALLOON CATHETER |
| Product Code | NUF |
| Date Received | 2011-10-12 |
| Returned To Mfg | 2011-09-13 |
| Model Number | 104-4112 |
| Lot Number | 9398916 |
| Device Expiration Date | 2013-10-01 |
| Operator | OTHER |
| Device Availability | Y |
| Device Eval'ed by Mfgr | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | EV3 NEUROVASCULAR |
| Manufacturer Address | 9775 TOLEDO WAY IRVINE CA 92618 US 92618 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2011-10-12 |