CARMEDA CIRCUIT - HEPARIN COATED Adverse Event — Other (MDR MW5005531)
CARMEDA CIRCUIT - HEPARIN COATED Adverse Event — Other (MDR MW5005531) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: CARMEDA CIRCUIT - HEPARIN COATED; Generic name: CARMEDA CIRCUIT - HEPARIN COATED; Manufacturer: MEDTRONIC.
| Device | CARMEDA CIRCUIT - HEPARIN COATED |
|---|---|
| Generic name | CARMEDA CIRCUIT - HEPARIN COATED |
| Manufacturer | MEDTRONIC |
| Report number | MW5005531 |
| Event type | Other |
| Product problem | Y |
| Date received | 2008-04-14 |
| Narrative | THIS WAS A NEWBORN WITH A LARGE DIAPHRAGMATIC HERNIA, WHO WAS PLACED ON EXTRACORPORAL MEMBRANE OXYGENATION - ECMO-. IMMEDIATELY AFTER ECMO WAS BEGUN, SHE DEVELOPED DIFFUSE PETECHIAL LESIONS WHICH PROGRESSED TO PURPURA AND HYPERTENSION, THEN DIC. SHE CONTINUED TO DETERIORATE AND DIED FROM HEMORRHAGE SECONDARY TO DIC. HEPARIN COATED CARMEDA TUBING WAS USED DURING ECMO AND THIS REPORT IS BEING FILED |
| Source | openFDA MAUDE (device adverse events) |
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