FOGARTY ARTERIAL EMBOLECTOMY CATHETER Adverse Event — Malfunction (MDR 6000002-1997-00486)
FOGARTY ARTERIAL EMBOLECTOMY CATHETER Adverse Event — Malfunction (MDR 6000002-1997-00486) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: FOGARTY ARTERIAL EMBOLECTOMY CATHETER; Generic name: EMBOLECTOMY CATHETER; Manufacturer: BAXTER HEALTHCARE CORP..
| Device | FOGARTY ARTERIAL EMBOLECTOMY CATHETER |
|---|---|
| Generic name | EMBOLECTOMY CATHETER |
| Manufacturer | BAXTER HEALTHCARE CORP. |
| Report number | 6000002-1997-00486 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 1997-06-18 |
| Report source | Health Professional, User facility |
| Narrative | WHEN CATHETER WAS REMOVED FROM THE ARTERY, AFTER THE THIRD PASS, THE BALLOON AND SPRING TIP WERE MISSING. UNABLE TO RETRIEVE. THERE WERE NO PT COMPLICATIONS OR INJURY. |
| Source | openFDA MAUDE (device adverse events) |
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