FREEDOM BED Adverse Event — Malfunction (MDR 8044130-2008-00001)
FREEDOM BED Adverse Event — Malfunction (MDR 8044130-2008-00001) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: FREEDOM BED; Generic name: PATIENT ROTATION BED; Manufacturer: PROBED MEDICAL TECHNOLOGIES, INC..
| Device | FREEDOM BED |
|---|---|
| Generic name | PATIENT ROTATION BED |
| Manufacturer | PROBED MEDICAL TECHNOLOGIES, INC. |
| Report number | 8044130-2008-00001 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-02-15 |
| Report source | Health Professional |
| Narrative | IN EARLY 2008, PROBED REC'D A CALL FROM REPORTER, ADVISING THAT OUR PROD, A FREEDOM BED HAD MALFUNCTIONED IN A HOME SETTING, WHERE THE PT HAS HOME CAREGIVERS. IT WAS REPORTED THAT THE CAREGIVER PRESSED THE HEAD DOWN BUTTON ON THE HAND CONTROL BUT THE HEAD WENT UP INSTEAD. THE BLOWER MOTOR THAT RAISES THE HEAD STAYED ON AND DID NOT QUIT WHEN SHE LET GO OF THE BUTTON (AS WOULD BE THE STANDARD PRACTI |
| Source | openFDA MAUDE (device adverse events) |
🔍 Search all device adverse events →
$1999/mo
Try DeviceEvents →