FOGARTY EMBOLECTOMY CATHETER Adverse Event — Malfunction (MDR 6000002-2008-06062)
FOGARTY EMBOLECTOMY CATHETER Adverse Event — Malfunction (MDR 6000002-2008-06062) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: FOGARTY EMBOLECTOMY CATHETER; Generic name: EMBOLECTOMY CATHETER; Manufacturer: EDWARDS LIFESCIENCES.
| Device | FOGARTY EMBOLECTOMY CATHETER |
|---|---|
| Generic name | EMBOLECTOMY CATHETER |
| Manufacturer | EDWARDS LIFESCIENCES |
| Report number | 6000002-2008-06062 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-02-18 |
| Report source | Health Professional, User facility, Company representation |
| Narrative | IT WAS REPORTED THAT AFTER THREE BALLOONS RUPTURED, 120404F WAS USED AND THE BALLOON DETACHED WHEN THE CUSTOMER PULLED THE CATHETER OUT. |
| Source | openFDA MAUDE (device adverse events) |
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