ECLIPSE Adverse Event — Malfunction (MDR MW5005579)
ECLIPSE Adverse Event — Malfunction (MDR MW5005579) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: ECLIPSE; Generic name: ELASTOMERIC DEVICE; Manufacturer: B BRAUN MEDICAL INC.
| Device | ECLIPSE |
|---|---|
| Generic name | ELASTOMERIC DEVICE |
| Manufacturer | B BRAUN MEDICAL INC |
| Report number | MW5005579 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-02-15 |
| Narrative | WE HAVE COLLECTED REPORTS OF FAILURE OF THE ECLIPSE E251750 DEVICE FROM 11 DIFFERENT PTS AT DIFFERENT SITES OF SERVICE WITHIN OUR COMPANY, BETWEEN SEPTEMBER 2007 AND TODAY. THE DEVICE FAILS TO INFUSE, RESULTING IN A MISSED DOSE. ONE PT REPORTED MULTIPLE DEVICE FAILURES IN A ROW. THE PROBLEMS HAVE BEEN REPORTED TO THE B BRAUN COMPANY AS THEY OCCURRED. THESE DEVICES WERE USED IN THE HOME CARE SETTIN |
| Source | openFDA MAUDE (device adverse events) |
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