GUIDANT VASO VIEW HEMOPRO Adverse Event — Malfunction (MDR 2953148-2008-00159)
GUIDANT VASO VIEW HEMOPRO Adverse Event — Malfunction (MDR 2953148-2008-00159) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: GUIDANT VASO VIEW HEMOPRO; Manufacturer: GUIDANT CARDIAC SURGERY; Report number: 2953148-2008-00159.
| Device | GUIDANT VASO VIEW HEMOPRO |
|---|---|
| Manufacturer | GUIDANT CARDIAC SURGERY |
| Report number | 2953148-2008-00159 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-02-15 |
| Report source | Health Professional, User facility, Company representation |
| Narrative | THE HOSPITAL REPORTED THAT DURING PREPARATION OF THE ENDOSCOPIC VEIN HARVESTING PROCEDURE, THE DEVICE WOULD NOT POWER UP. A REPLACEMENT UNIT WAS USED TO COMPLETE THE PROCEDURE. THEN THE HOSPITAL REPORTED THAT DURING PREPARATION FOR THE CORONARY ARTERY BYPASS GRAFT PORTION OF THE SURGERY, TWO HEARTSTRING SEALS CRACKED WHILE LOADING THE SEALS INTO THE DELIVERY TUBE. THE SURGEON USED A REPLACEMENT HE |
| Source | openFDA MAUDE (device adverse events) |
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